AU2005233039A1 - Indene derivatives and process for the preparation thereof - Google Patents

Indene derivatives and process for the preparation thereof Download PDF

Info

Publication number
AU2005233039A1
AU2005233039A1 AU2005233039A AU2005233039A AU2005233039A1 AU 2005233039 A1 AU2005233039 A1 AU 2005233039A1 AU 2005233039 A AU2005233039 A AU 2005233039A AU 2005233039 A AU2005233039 A AU 2005233039A AU 2005233039 A1 AU2005233039 A1 AU 2005233039A1
Authority
AU
Australia
Prior art keywords
indene
oxy
phenyl
trans
methylimino
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
AU2005233039A
Other versions
AU2005233039B2 (en
Inventor
Jin Hee Ahn
Hyae Gyeong Cheon
Sun Chul Huh
Won Hoon Jung
Seung Kyu Kang
Jong Hoon Kim
Kwang-Rok Kim
Nam Gee Kim
Seung Jun Kim
Sung Soo Kim
Soon Ji Kwon
Jae Mok Lee
Jang Hyuk Lee
Jeong-Hyung Lee
Sung Dae Park
Sang Dal Rhee
Seog Beom Song
Sung-Don Yang
Sung-Eun Yoo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CJ Corp
Korea Research Institute of Chemical Technology KRICT
Korea Research Institute of Bioscience and Biotechnology KRIBB
Jeil Pharmaceutical Co Ltd
Original Assignee
CJ Corp
Korea Research Institute of Chemical Technology KRICT
Korea Research Institute of Bioscience and Biotechnology KRIBB
Jeil Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CJ Corp, Korea Research Institute of Chemical Technology KRICT, Korea Research Institute of Bioscience and Biotechnology KRIBB, Jeil Pharmaceutical Co Ltd filed Critical CJ Corp
Publication of AU2005233039A1 publication Critical patent/AU2005233039A1/en
Application granted granted Critical
Publication of AU2005233039B2 publication Critical patent/AU2005233039B2/en
Ceased legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/32—Oximes
    • C07C251/34—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • C07C251/44—Oximes with oxygen atoms of oxyimino groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with the carbon atom of at least one of the oxyimino groups being part of a ring other than a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/15—Oximes (>C=N—O—); Hydrazines (>N—N<); Hydrazones (>N—N=) ; Imines (C—N=C)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/06—Antihyperlipidemics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
    • A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/12—Antihypertensives
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C291/00—Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00
    • C07C291/02—Compounds containing carbon and nitrogen and having functional groups not covered by groups C07C201/00 - C07C281/00 containing nitrogen-oxide bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/63—Esters of sulfonic acids
    • C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
    • C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
    • C07C309/66—Methanesulfonates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/53—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/24—Radicals substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182—Radicals derived from carboxylic acids
    • C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/60—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/70—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with ring systems containing two or more relevant rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/28—Halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/56—Ring systems containing bridged rings
    • C07C2603/58—Ring systems containing bridged rings containing three rings
    • C07C2603/70—Ring systems containing bridged rings containing three rings containing only six-membered rings
    • C07C2603/74—Adamantanes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Hematology (AREA)
  • Rheumatology (AREA)
  • Epidemiology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Endocrinology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
  • Pain & Pain Management (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Child & Adolescent Psychology (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

WO 2005/100303 PCT/KR2005/001066 1 INDENE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF Field of the Invention 5 The present invention relates to a novel indene derivative, which is useful as a modulator of peroxisome proliferator activated receptors (PPARs), a process for the preparation thereof and a pharmaceutical composition containing same as an active ingredient. 10 Background of the Invention Peroxisome proliferator activated receptors (PPARs) are members of the nuclear hormone receptor superfamily and function as transcription factors 15 regulating gene expression in the form of heterodimers with retinoid X receptors (RXRs). The PPARs are divided into three subtypes, "PPAR a ", "PPAR y " and "PPAR 6 ", and are generally involved in maintaining energy homeostasis in vertebrates through the control of fat and glucose metabolisms. Accordingly, many attempts have been made to develop PPAR a and 20 PPAR y full agonists which are useful for the treatment and prevention of disorders modulated by PPARs, e.g., metabolic syndromes such as diabetes, obesity, arteriosclerosis, hyperlipidemia, hyperinsulinism and hypertension; inflammatory diseases such as osteoporosis, liver cirrhosis and asthma; and cancer. 25 For example, it has been reported that thiazolidine-2,4-dione (TZD) and non-TZD-based full agonists on PPAR y exhibit excellent blood glucose level lowering effect in non-insulin dependent diabetes mellitus (NIDDM) mammal models (J. Med. Chem., 1999, 42, 3785.; Bioorg. Med. Chem. Lett., 2000, 2453.; Chlem. Pharm. Bull., 2002, 50, 1349.; Bioorg. Med. Chem. Lett., 2002, 30 77.; J. Med. Chem., 2003, 46, 3581.). However, such PPAR y full agonists are also known to cause adverse side effects including weight gain due to facilitation of fat cell differentiation, cardiac hypertrophy, edema and liver damage.
WO 2005/100303 PCT/KR2005/001066 2 Therefore, there exists a need to develop selective PPAR modulators (SPPARMs), which are capable of selectively controlling the activities of the PPARs without causing side effects (Molecular Cell, 2001, 8, 737; Molecular Endocrinology, 2003, 17, 662; Molecular Endocrinology, 2002, 16, 2628). 5 Summary of the Invention Accordingly, it is a primary object of the present invention to provide a 10 novel compound, which is capable of selectively modulating the activities of peroxisome proliferator activated receptors (PPARs), causing no adverse side effects. It is another object of the present invention to provide a process for the preparation of said compound. 15 It is a further object of the present invention to provide a pharmaceutical composition containing said compound as an active ingredient. In accordance with one aspect of the present invention, there is provided a novel indene derivative of formula (I) or a pharmaceutically acceptable salt thereof: 20 O0 R7 cN+" R1 R6 RR2 R5 L R
R
4 R3 (I) wherein,
R
1 is C 1
_
6 alkyl, C1- 6 alkenyl or C 3
.
6 cycloalkyl, which is unsubstituted or substitutied with one or more phenyl groups; 0 25 R 2 is H, CN, CO 2 Ra, CH 2
CO
2 Ra, CONRbRC Rd, or phenyl; WO 2005/100303 PCT/KR2005/001066 3 0 (NI
R
3 is C 1
-
6 alkyl, C 3
-
6 cycloalkyl, or naphthyl, phenyl, , , or H , which is unsubstituted or substitutied with one or more substituents selected from the group consisting of halogen, CN,
NH
2 , NO 2 , ORa, phenyloxy, C 1 -6 alkyl and C 3
-
6 cycloalkyl; and 5 R 4 , Rs, R 6 and R 7 are each independently H, OH, OSO 2
CH
3 , O(CH 2 )mR e,
CH
2
R
f , OCOCH2OR g, OCH2CH2OR or OCH2CH=CHR g, or R 5 and R 6 together form OCH 2 0; in which Ra is H, or C 1
.
6 alkyl or C 3
-
6 cycloalkyl, which is unsubstituted or substitutied with one or more halogens; 10 Rb and R e are each independently H, C 1 -6 alkyl or C 3
-
6 cycloalkyl;
R
d is O, S or NRa; Re is H, halogen, C 3
-
6 cycloalkyl, naphthyl,
R
a N Ra N , , , or phenyl, which is unsubstituted or substituted with one or more substituents selected from the 15 group consisting of halogen, CN, NH 2 , NO 2 , ORa, CF 3 and COORa; + -j- R' R is OCH 2
CH
2
R
g or ; R9 is phenyl, which is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, CN, NH 2 , NO 2 and ORa; and 20 m is an integer in the range of 1 to 5. Detailed Description of the Invention The indene derivatives of the present invention may include optical WO 2005/100303 PCT/KR2005/001066 4 isomers of the compound of formula (I). The pharmaceutically acceptable salt of the inventive indene derivative is a non-toxic addition salt generated from an inorganic acid such as hydrochloric acid, an organic acid such as trifluoroacetic acid, citric acid, lactic acid, maleic 5 acid and fumaric acid, an inorganic base such as an alkali or alkaline earth metal (e.g., sodium, potassium, magnesium and calcium) hydroxides, bicarbonates and carbonates, or an organic base such as amines. Among the compounds of formula ( I ) of the present invention, preferred are those wherein R, is C1- 6 alkyl, which is unsubstituted or 10 substitutied with a phenyl group; R 2 is H, CN, CO 2 Ra, CH 2
CO
2 Ra, CONRbR or phenyl; R 3 is C1-6 alkyl, C 3
.
6 cycloalkyl, or phenyl, 0 N 0 S SN , , , , or H , which is unsubstituted or substitutied with one or more substituents selected from the group consisting of halogen, C 1
-
6 alkyl and C 3
.-
6 cycloalkyl; R 4 and R 7 are H; Rs and R 6 are each 15 independently OH, OSO 2
CH
3 , O(CH 2 )mRe, CH 2 R', OCOCH20R9, OCH2CH2OR9 or OCH2CH=CHR' , or together form OCH 2 0; Ra is H, or Cl-6 alkyl; Rd is O or NCH 3 ; Re is H, halogen, C 3
.-
6 cycloalkyl, naphthyl, N R , , , , or phenyl, which is unsubstituted or substituted with one or more substituents selected from the 20 group consisting of halogen, OH, methoxy, CF 3 and COORa; R f is OCH 2
CH
2
R
g --N Rd or ; and R g is phenyl. More preferred are those wherein R 1 is CH 3 ; R 2 is H, CN, CO 2 Ra or CONRbR; R 3 is C 1
-
6 alkyl, or phenyl, , , , , WO 2005/100303 PCT/KR2005/001066 5 /I-N N or H , which is unsubstituted or substitutied with one or more halogens or
C
1 -6 alkyl groups; and R 5 and R 6 are each independently O(CH 2 )mRe or CH 2
R
f, or together form OCH 2 0. 5 The present invention also provides processes for preparing indene derivatives of formula (I). The inventive compound of formula (I) may be prepared, for example, as shown in Reaction Scheme ( I): 10 Reaction Scheme ( I)
R
7 0 R 7 %N- RI R 7 W R6 R2 R 1 NHOH R R 6 R2/
R
5 F 2 /R R 5 /
R
4
R
3 3R R3 I II I (trans) I (cIs) 20 NH 2 0H HO RO 0'7
R
7 N RR 7 -X RR OR R R R 2 + R 2 R5 RR 3 R R3 mI IV I 25 wherein, R, to R 7 have the same meanings as defined in formula (I ), and X is halogen. In Reaction Scheme ( I), a compound of formula (II) may be stirred 30 with alkyl hydroxylamine having various substituents or its hydrochloride salt WO 2005/100303 PCT/KR2005/001066 6 in the presence of a suitable base under a nitrogen atmosphere to obtain a compound of formula ( I ) until the compound of formula (II) is entirely consumed. At this time, 2 to 10 equivalents of alkyl hydroxylamine or its hydrochloride is used, and cis and trans compounds (geometric isomers) of 5 formula ( I ) are obtained together. Examples of the desirable reaction solvent that can be used in this reaction are dimethylformamide, nitroethane, methanol or ethanol, and 2 to 10 equivalents of amines such as 2,6-lutidine or pyridine is used at a temperature in the range of 50 to 120 C for 12 to 36 hours, preferably in a pressure reactor. 10 Alternatively, a compound of formula ( II) can be stirred with hydroxylamine or its hydrochloride salt under in the presence of a suitable base to obtain a compound of formula (III) until the compound of formula (II) is entirely consumed. In this reaction, 2 to 10 equivalents of hydroxylamine or its hydrochloride salt is used. Examples of the desirable reaction solvent can 15 be used in this reaction are methanol and ethanol, and 2 to 10 equivalents of amines such as pyridine is used at a temperature of 20 to 100 C for 3 to 12 hours. Also, a compound of formula (I) can be reacted with 1 to 3 equivalents of alkyl halide in a solvent such as dimethyl formamide or acetone in the 20 presence of an inorganic base such as potassium carbonate to obtain a compound of formula ( I ). At this time, the alkoxy imine form of the compound of formula (1V) is synthesized together. In case the compound of formula ( I ) is synthesized according to Reaction Scheme ( I ), a mixture of geometric isomers comprising cis and trans 25 compounds about the imine double bond is obtained, and each pure isomer can be isolated by column chromatography. Each of the cis and trans isomer can be converted to the other isomer under suitable reaction condition. For example, the cis or trans compound is converted partly to the other isomer when it is stirred for a long period of time in the presence of an inorganic base 30 such as lithium hydroxide in an alcohol solvent such as methanol or ethanol. Most of the cis isomer is converted to the trans isomer in 1-2 hours when it is WO 2005/100303 PCT/KR2005/001066 7 heated at 110 °C in an organic solvent such as benzene, toluene or xylene. A similar isomer conversion reaction can be carried out phtochemically when an isomer is irradiated with intense visible or ultraviolet light. The compound of formula (II) may be obtained by the method 5 described in Tetrahedron, 1995, 51, 12179; J. Org. Chem., 1993, 58, 4579; J Chemn. Soc., Perkin Trans I., 1992, 2985; Synthesis, 1991, 115 & 176; J Med. Chem., 1998, 31, 1316 & 1754, as shown in Reaction Schemes (II) to (VII). Reaction scheme (II) 10 R7 R e'N Z R 7 R2 0. R R F) r
R
3 R2 ' R RR" - 0 R3 V VI R 4 V ~VH I PPA
R
7
R
7 0 R R /R 2 SeO2
R
2
R
5
R
3 R 4
R
3
R
4 R3 II VIII wherein,
R
2 to R 7 have the same meanings as defined in formula ( I ), and Z is halogen or an activated leaving group. 30 1) The compounds of formula (V) and (VI), which are commercially available or easily prepared in accordance with the conventional procedures, may be reacted with each other to obtain the compound of formula (VII). Z of the compound of formula (VI) is halogen or an activated leaving group such as methane sulfonate. 2 to 10 equivalents of an inorganic base such as potassium 35 carbonate, and a polar solvent such as acetone or dimethyl formamide are WO 2005/100303 PCT/KR2005/001066 8 perferably used. If necessary, 1-3 equivalents of sodium iodide or potassium iodide are added to facilitate the reaction. Desirably, the reaction is carried out at 20 to 50'C for 3 to 15 hours. 2) The compound of formula (VII) may be reacted with polyphosphoric 5 acid (PPA) which also acts as a solvent (5-10 equivalents) at 30 to 50 C for a period of 3 to 12 hours to obtain the cyclized compound of formula (VIII). Xylene may be used as a co-solvent, and methane sulfonic acid (MSA) or pyridium toluene sulfonate (PPTS) may be used in place of polyphosphoric acid under different conditions. 10 3) The compound of formula (VIl) may be oxidized to the compound of formula (II) by using a common oxidant. For example, an excess amount (5 15 equivalents) of selenium dioxide as the most preferable oxidant may be used in a solvent such as 1,4-dioxane or tetrahydrofuran at 50-120 C for 7-15 hours to obtain the oxidized compound of formula (II). 15 Reaction Scheme (IfI)
R
7 O O R 7 0 R5
R
2 R4 IX R4 X I MSA So R 7 , R N P iSeCI RN R6 R R5 - I R4RP 2 Khel R1 z 3R IIX II wherein,
R
2 to R 7 have the same meanings as defined in formula ( I ). 20 In the first step of Recation Scheme (III), equivalent amounts of compounds of formula (IX) and (X), which are commercially available or WO 2005/100303 PCT/KR2005/001066 9 easily prepared in accordance with the conventional procedures, may be subjected to a condensation reaction to obtain the compound of formula (XI) in the presence of 2 to 5 equivalents of an amine base such as piperidine or an inorganic base such as sodium hydroxide using a polar solvent such as 5 dimethylformamide, ethanol or nitroethane. Desirably, the reaction is carried out at 20 to 80'C for 3 to 15 hours. In the second step, the compound of formula (XI) is reacted with an excess amount of methane sulfonic acid (MSA), pyridinium toluene sulfonate (PPTS) or polyphosphoric acid (PPA) at 20 to 50 C for 3 to 12 hours in a 10 solvent such as dichioromethane, chloroform, carbon tetrachloride or xylene, to obtain the cyclized compound of formula (XII). In case the compound of formula (XI) is reacted with aluminum chloride in anhydrous nitroethane under a nitrogen gas, it is subjected to the both condensation and cyclization reactions to obtain the compound of formula (XII). 15 In the third step, the compound of formula (XII) is oxidized to the compound of formula (1I) using a common oxidants such as phenyl selenium chloride and hydrogen peroxide. The compound of formula (X II) is reacted with 1-3 equivalents of selenium dioxide in the presence of an amine base such as 1-5 equivalents of pyridine. An excess amount of 30 % hydrogen peroxide 20 may be added to obtain the compound of formula (II) in a high yield. The reaction may be carried out in a solvent such as dichloromethane, chloroform, carbon tetrachloride or 1,4-dioxane at 20-70 C for 3-15 hours. Reaction Scheme (IV)
R
7
R
7 R Re R R )CI XIIIRe PPA Re 2 Rs-R5 -0 R3 or M6A R 5
R
4 44 30 IX X1V II wherein,
R
2 to R 7 have the same meanings as defined in formula ( I ).
WO 2005/100303 PCT/KR2005/001066 10 In the first step of Reaction Scheme (IV), equivalent amount of compounds of formula (IX) and (XIII), which are commercially available or easily prepared in accordance with the conventional procedures, are subjected to a condensation reaction to obtain the compound of formula (XIV). 2 to 5 5 equivalents of an amine base such as piperidine and an inorganic base such as sodium hydroxide, and a solvent such as tetrahydrofuran or dimethyl formamide may be used in the reaction which is preferably carried out at 20 to 70 C for 3 to 15 hours. In the second step, the compound of formula (XIV) is reacted with an 10 excess amount of methanesufonic acid (MSA), pyridinium toluene sulfonate (PPTS) or polyphosphoric acid (PPA) at 20 to 50 'C to obtain the cyclized compound of formula (II). The reaction may be carried out in dichloromethane, chloroform, carbon tetrachloride or xylene for 3 to 12 hours. 15 Reaction Scheme (V) R7 olR7 0R 7 o0 Re NBS R Pd reaction Re R Re Br o Re
R
4 R3 4 R 3
R
4 R3 XV XVI H wherein,
R
2 to R 7 have the same meanings as defined in formula ( I). 25 In the first step of Reaction Scheme (V), the compound of formula (XV), which is commercially available or easily prepared in accordance with the conventional procedures is subjected to bromination to obtain the compound of formula (XVI) by treating with 1 to 3 equivalents of N-bromosuccinimide (NBS) in carbon tetrachloride under infrared irradiation at 50 to 100 0 C, for 0.5 30 to 3 hours. The compound of formula (XVI) can also be obtained by using a catalytic amount of a radical reaction initiator (e.g., azobisisobutyronitrile) instead of infrared irradiation.
WO 2005/100303 PCT/KR2005/001066 11 In the second step, the compound of formula (XVI) is subjected to a carbon-carbon coupling reaction in the presence of a palladium catalyst to obtain the compound of formula (II) according to the procedure of the well known Suzuki reaction or Heck reaction. 5 Also, the bromine substituent of the compound of formula (XVI) may be replaced with R 3 using a suitable nucleophilic agent. The compound of formula (XVI) may be reacted with 1-5 equivalents of copper ( I ) cyanide or sodium methane sulfonate at 70-150°C in a polar solvent such as nitroethane or dimethylfonnamide for 3-15 hours to obtain the compound of formula (II) 10 Reaction Scheme (VI)
R
7 o R D R 7 0 Pd reaction R 5 R6 NSS R5 R / R 2 orRR "rRR
R
4
R
4 Br R4 XVII XVIII 20 wherein,
R
2 to R 7 have the same meanings as defined in formula ( I ). In the first step of Reaction Scheme (VI), the compound of formula (XVII), which is synthesized as an intermediate in Reaction Schemes (II) to (V) or easily prepared in accordance with the conventional procedures, is 25 brominated to obtain the compound of formula (XVIII) using 1-3 equivalents of N-bromosuccinimide (NBS) in carbon tetrachloride under infrared irradiation. This reaction may be carried out at 50 to 1001C for 0.5 to 3 hours. The compound of formula (XVIII) can also be obtained by using a catalytic amount of a radical reaction initiator (e.g., azobisisobutyronitrile) instead of infrared 30 irradiation. In the second step, the compound of formula (XVIII) may be subjected to a carbon-carbon coupling reaction using a palladium catalyst according to the procedure of Suzuki reaction, Heck reaction or Stille reaction to obtain the compound of formula (II) having various substituents at R 3
.
WO 2005/100303 PCT/KR2005/001066 12 Also, the bromine substituents of the compound of formula (XVIII) may be replaced with R 3 using a suitable nucleophilic agent. The compound of formula (XVII) may be reacted with 1-5 equivalents of cupper cyanide, sodium methane sulfonate, amine or alkoxide in a polar solvent such as nitroethane or 5 dimethylformamide at 70-150 C for 3-15 hours to obtain the compound of formula (HI). In case the benzene ring of indene of formula (II) obtained in Reaction Schemes (II) to (VI) has a hydroxy, thiol, amino, alkyl, halogen or alkyl hydroxy substituents, various substituents can be further introduced to the 10 benzene ring of the indene according to Reaction Scheme (VII). Reaction Scheme (VII) to 5. 20 In case that Y of the compound of formula ( X IX) is hydroxy, thiol or amino, the compound may be acylated with various carboxylic acids or derivatives thereof to obtain the compound of formula (II) having various substituents. When a carboxylic acid is used in the acylation, the compound of formula (XIX) is reacted with equal amounts of a carboxylic acid and a 25 condensation reagent such as dicyclohexylcarbodiimide (DCC) in dichloromethane at room temperature for 1-12 hours to obtain the compound of Y -(H ) - -Z; / 'I / R XKI 15 wherein,
R
2 to R 7 have the same meanings as defined in formula I). Y is hydroxy, thiolen amin aci d c hloride is used, an equivale integer in the range of an acid to 5. 20 In case that Y of the compound of formula (X IX) is hydroxy, thiol or amino, the compound may be acylated with various carboxylic acids or derivatives thereof to obtain the compound of formula (HI) having various substituents. When a carboxylic acid is used in the acylation, the compound of formula (XIX) is reacted with equal amounts of a carboxylic acid and a 25 condensation reagent such as dicyclohexylcarbodiimide (DCC) in dichioromethane at room temperature for 1-12 hours to obtain the compound of formula (H). When anl acid chloride is used, an equivalent amount of an acid WO 2005/100303 PCT/KR2005/001066 13 chloride and 1-2 equivalents of an amine base such as triethylamine and pyridine are used to carry out the reaction in dichloromethane at 0-30 0 C for 1-5 hours to obtain the compound of formula (II). Also, the compound of formula (II) having an introduced sulfide, ether 5 or alkylamino group may be obtained easily by a conventional alkylation reaction such as Mitsunobu reaction. In Mitsunobu reaction, 1-3 equivalents of an alcohol, triphenyl phosphine, and DEAD (diethyl azodicarboxylate) or DIAD (diisopropyl azodicarboxylate) are stirred in tetrahydrofuran or benzene at 0-30'C for 1-12 hours to obtain the compound of formula (II). 10 In addition, the compound of formula (H) may be obtained by alkylating with haloalkyl substituted with an alkyl or aryl group in the presence of a base such as sodium hydride, potassium carbonate and sodium hydroxide, in acetone or N,N-dimethylformamide at 20-100 'C for 3-12 hours. 2) In case that Y of the indene compound of formula (XIX) is C 1
-
6 alkyl, 15 a halogen substituents may be introduced by halogenation, and then substituting the halogen with a suitable nucleophile to obtain the compound of formula ( II). The halogenation may be conducted in a conventional way. For example, bromination may be conducted using 1-3 equivalents of NBS in carbon tetrachloride under infrared irradiation at 50 to 100 C for 0.5 to 3 hours. The 20 bromination can also be conducted using a catalytic amount of a radical reaction initiator (e.g., azobisisobutyronitrile) instead of infrared irradiation. The intermediate obtained by halogenation may be subjected to a substitution reaction an alkyl, aryl or heterocycle compound having various substituents such as hydroxy, amino, thiol, or carboxylic acid substituents under 25 conventional reaction conditions to obtain the title compound of formula (II). Generally, the reaction is conducted with 1-2 equivalents of the nucleophile in a solvent such as dichloromethane, tetrahydrofuran or dimethylformamide in the presence of 1-3 equivalents of an inorganic base such as potassium carbonate or amine base such as triethylamine at 0-70 C for 1-7 hours. 1-3 equivalents of 30 sodium iodide may be added to enhance the reaction. The compound of formula (XIX) may also be subjected to a carbon- WO 2005/100303 PCT/KR2005/001066 14 carbon coupling reaction using a palladium catalyst according to the procedure of Suzuki reaction, Heck reaction or Stille reaction to obtain the compound of formula (II) having various substituents such as alkyl, aryl or heterocycle, when n and Y of the indene of formula (XIX) are 0 and halogen, respectively. 5 Exemplary compounds of formula (I) of the present invention, which can be prepared in accordance with the methods described above, are listed in Table 1: 10 WO 2005/100303 PCT/KR2005/001066 15 Table 1 No. structure 1 H-NMR (CDCI 3 , 300 MHz) 6 o.- 8.28 (d, J=2.4Hz, 1H), 7.44 - 7.42 (m, 5H), 7.16 (d, J = 8.4 Hz, 1H), 6.86 (dd, o-\ J=8.4Hz, J=2.4Hz, 1H), 4.16 (q, J = 7.1 Hz, 2H), 4.13 (s, 3H), 3.89 (s, 3H), - 1.05 (t, J=7.1Hz, 3H) o:,a 8.41 (d, J= 2.2Hz, 1H), 7.45 (s, 5H), 7.17 (d, J= 8.4Hz, 1H), 6.89 (dd, J= 8.4, /O 0 2 0. 2.4Hz, 1H), 4.90 - 4.80 (m, 1H), 4.15 (q, J=7.0Hz, 2H), 3.91 (s, 3H), 1.53 (d, J=6.3 Hz, 6H), 1.06 (t, J= 7.1Hz, 3H) o 8.38 (d, J=2.2Hz, 1H), 7.43 - 7.34 (m, 10H), 7.16 (d, J=8.6Hz, 1H), 6.80 (dd, J 3 , o = 8.3, 2.2 Hz, 1H), 5.55 (s, 2H), 4.01 (q, J = 7.1 Hz, 2H), 3.86 (s, 3H), 0.89 (t, 0--\ S - J=7.1Hz, 3H) o 8.35 (d, J=2.2Hz, 1H), 7.43 (s, 5H), 7.16 (d, J=8.2Hz, 1H), 6.86 (dd, J=8.4, 2.2 4 , o Hz, 1H), 4.28 (q, J=7.0 Hz, 2H), 4.12 (q, J=7.0 Hz, 2H), 3.89 (s, 3H), 1.25 (t, J = 7.0 Hz, 3H), 1.03 (t, J=7.1Hz, 3H) 8.34 (d, J=2.2Hz, 1H), 7.43 (s, 5H), 7.27 - 7.13 (m, 6 H), 6.87 (dd, J = 8.3, 5O S ,.o o 2.2Hz, 1H), 4.27 (t, J=6.4Hz, 2H), 4.03 (q, J = 7.0 Hz, 2H), 3.89 (s, 3H), 2.73 (t, J = 6.4 Hz, 2H), 2.42 -2.36 (m, 2H), 0.97 (t, J = 7.0 Hz, 3H) o 8.33 (d, J=2.6Hz, 1H), 7.43 (s, 5H), 7.15 (d, J=8.4Hz, 1H), 6.83 (q, J = 8.4, 2.6 6 o1 Hz, 1H), 5.50 (t, J= 6.5 Hz, 1H), 4.92 (d, J=6.5 Hz, 2H), 4.09 (q, J= 7.0 Hz, 0--\ /2H), 3.87 (s, 3H), 1.79 (d, J=2.2 Hz, 6H), 1.00 (t, J = 7.0 Hz, 3H) 8.37 (d, J=2.6Hz, 1H), 7.43 (s, 5H), 7.17 (d, J=8.4Hz, 1H), 6.86 (dd, J=8.4, 0 7 1 J=2.6Hz, 1H), 4.35 - 4.04 (m, 4H), 3.89 (s, 3H), 2.45 (m, 1H), 1.05-0.97 (m, lot, o 9H) S8.27 (d, J = 2.6 Hz, 1H), 7.49 - 7.31 (m, 5H), 7.13 (d, J = 8.2 Hz, 1H), 6.85 (dd, S0 J = 8.2, 2.6 Hz, 1H), 5.02 (sept, J=6.6 Hz, 1H), 4.27-4.10 (m, 5H), 3.74 (t, 8 0 a J=4.6 Hz, 4H), 2.83 (t, J = 5.6 Hz, 2H), 2.59 (t, J = 4.6 Hz, 4H), 1.05 (d, J=6.6 Hz, 6H), mp 79-81 'C WO 2005/100303 PCT/KR2005/001066 16 No. structure 'H-NMR (CDCI 3 , 300 MHz) 6 0 o. - 8.27 (d, J= 2.2 Hz, 1H), 7.43 (s, 5H), 7.31 - 7.17 (m, 5H), 7.15 (d, J= 8.1 Hz, 1 9 - o- 1H), 6.84 (dd, J = 8.2, 2.2 Hz, 1H), 4.16 - 4.03 (m, 7H), 2.82 (t, J= 7.1 Hz, 2H), 2.20 - 2.10 (m, 2H), 1.04 (t, J" = 7.1 Hz, 3H) 0, 8.30 (d, J = 2.4 Hz, 1H), 7.51 - 7.24 (m, 10H), 7.16 (d, J = 8.3 Hz, 1H), 6.85 0 / 0 10 a\ _ (dd,J=8.3,2.4Hz, 1H),4.31-4.08(m,7H),3.13(t,J=7.1 Hz,2H), 1.05(t,J =7.1 Hz, 3H) . 8.28 (d, J = 2.4 Hz, 1H), 7.86 (dd, J =1.4, 0.8 Hz, 1H), 7.54 (dd, J =1.8, 1.4 o Hz, 1I), 7.38 - 7.19 (m, 6H), 6.90 (dd, J = 8.4, 2.4 Hz, 1H), 6.68 (dd, J= 1.8, S 0.8 Hz, 1H), 4.31 (q, J = 7.1 Hz, 2H), 4.1 - 4.01 (m, 5H), 2.84 (t, 2H), 2.20 0 2.10 (m, 2H), 1.28 (t, J= 7.1 Hz, 3H) 0, o . 9.42 (brs, 1H), 8.60 (d, J 2.2 Hz, 1H), 7.44 (s, 5H), 7.11 (d, J= 8.2 Hz, 1H), 012 " oo_ 6.85 (dd, J= 8.2,2.2 Hz, 1H), 4.14 (q, J= 7.1 Hz, 2H), 1.03 (t, J = 7.1 Hz, 3H) 0 1o 7.57 - 7.53 (m, 2H), 7.47 - 7.40 (m, 3H), 7.32 - 7.20 (m, 6H), 7.08 (d, J = 1.9 0 0 1 .- Hz, 1H), 6.74 (dd, J= 8.6, 1.9 Hz, 1H), 4.27 (q, J = 7.1 Hz, 2H), 4.24 (s, 3H), 13 o O 4.01 (t, J =6.4 Hz, 2H), 2.84 (t, J = 7.5 Hz, 2H), 2.84 (t, J = 7.5 Hz, 2H), 2.20 2.10 (m, 2H), 1.24 (t, J= 7.1 Hz, 3H) 0 14 0 9.69 (br, 1H), 8.59 (s, 1H), 7.64 - 7.36 (m, 5H), 7.38 (d, J = 8.2 Hz, 1H), 6.85 14/ (dd, J= 8.2, 2.2 Hz, 1H), 6.29 (s, 1H), 4.13 (s, 1H) 8.26 (d, J=2.4Hz, IH), 7.44 - 7.42 (m, 5H), 7.28 - 7.13 (m, 6H), 6.83 (dd, a J=8.4, 2.4Hz, 1H), 4.16 -4.08 (m, 5H), 4.04 (t, J= 6.6 Hz, 2H), 2.65 (t, J=7.2 15 Hz, 2H), 1.90 - 1.80 (m, 2H), 1.70 - 1.64 (m, 2H), 1.60 - 1.50 (m, 2H), 1.04 (t, J=7.1Hz, 3H) 7.57 - 7.54 (m, 2H), 7.43 - 7.41 (m, 3H), 7.31 - 7.07 (m, 6H), 7.07 (d, J = 2.1 16 o o- Hz, 1H), 6.77 (dd, J=8.4, 2.1 Hz, 1H), 4.30 - 4.28 (m, 5H), 3.99 (t, J = 6.6 Hz, 16 / 0 2H), 2.66 (t, J=7.2 Hz, 2H), 1.90- 1.80 (m, 2H), 1.73 - 1.66 (m, 2H), 1.59 1.51 (m, 2H), 1.25 (t, J=7.1Hz, 3H) WO 2005/100303 PCT/KR2005/001066 17 No. structure 1 H-NMR (CDC 3 la, 300 MHz) 6 cl, O. 8.37 (d, J=2.1Hz, 1H), 7.45 - 7.42 (mn, 5H), 7.30 - 7.26 (m, 3H), 7.11 (dd, 17 a . / J=8.1, 2.1Hz, 1H), 6.93 (d, J=8.7Hz, 2H), 4.88 (s, 2H), 4.19 - 4.09 (m, 5H), 1.06 (t, J=7.1Hz, 3H) 18 o ao a 8.32 (d, J=2.4Hz, 1H), 7.44 (s, 5H), 7.29 - 7.16 (m, 3H), 6.94 - 6.87 (m, 3H), S4.44 - 4.19 (m, 4H), 4.17 - 4.07 (m, 5H), 1.05 (t, J = 7.1 Hz, 3H) o8.44 (d, J=2.8Hz, 1H), 7.92 - 7.82 (m, 4H), 7.59 - 7.44 (m, 8H), 7.18 (d, J= 19 \ 8.3 Hz, 1H), 6.96 (dd, J=8.4, 2.6 Hz, 1H), 5.32 (s, 2H), 4.19 - 4.07 (m, 5H), 1.05 (t, J=7.0 Hz, 3H) . 8.22 (d, J = 2.4 Hz, 1H), 7.65 - 7.18 (m, 11H), 6.87 (dd, J = 8.3, 2.4 Hz, 1H), 20 6.41 (s, 1H), 4.12 (s, 3H), 4.07 (t, J = 6.2 Hz, 2H), 2.83 (t, J 7.2 Hz, 2H), 2.12 (m, 2H) o 8.28 (d, J= 2.4 Hz, 1H), 7.88 - 7.85 (m, 2H), 7.43 - 7.36 (m, 8H), 7.14 (d, J = 8.1 Hz, 1H), 6.85 (dd, J= 8.1, 2.4 Hz, 1H), 4.41 (t, J= 6.9 Hz, 2H), 4.12 (q, J= 210 21 N \ 7.1 Hz, 2H), 4.11 (s, 3H), 3.22 (t, J= 6.6 Hz, 3H), 2.47 (s, 3H), 1.04 (t, J= 7.1 Hz, 3H) o a 8.27 (d, J=2.0Hz, 1H), 8.27 (s, 5H), 7.29 - 6.81 (m, 7H), 4.11 (s, 3H), 4.06 (t, 22 . S J=6.3Hz, 2H), 3.67 (s, 3H), 2.83 (t, J=7.1Hz, 2H), 2.13 (quint, J=6.5Hz, 2H) o a 8.28 (d, J=2.4Hz, 1H), 7.43 (s, 5H), 7.25 - 7.07 (m, 3H), 6.86 - 6.76 (m, 3H), 23 o 5.09 (brs, 1H), 4.27 - 4.03(m, 7H), 3.04 (t, J=7.0Hz, 2H), 1.04 (t, J=7.1Hz, 3H) 24 .. 0 8.26 (d, J=2.4Hz, 1H), 7.43 (m, 5H), 7.18 (d, J = 8.2 Hz, 1H), 6.83 (dd, J=8.2, - a 2.4Hz, 1H), 4.29 - 4.04(m, 7H), 1.96 - 1.50 (m,15H), 1.04 (t, J=7.1Hz, 3H) WO 2005/100303 PCT/KR2005/001066 18 No. structure 1H-NMR (CDCI 3 , 300 MHz) 8 0 o 8.26 (d, J=2.2Hz, 1H), 7.43 (m, 5H), 7.25 (d, J = 8.2 Hz, 1H), 6.84 (dd, J=8.2, 25 a 25 c -\ 2.2Hz, 1H), 4.28 - 4.04(m, 7H), 1.79 - 0.76 (m, 13H) 0o 8.35 (d, J=2.4Hz, 1H), 7.44 - 7.12 (m, 11H), 6.91 (dd, J=8.4, 2.4Hz, 1H), 6,77 26 o- (d, J=15.8Hz, 1H), 6.47 - 6.41 (m, 1H), 4.82 - 4.76 (mn, 2H), 4.29 - 4.08 (m, S 5H), 1.05 (t, J=7.2Hz, 3H) 0, 27 , N / 8.27 (d, J=2.4Hz, 1H), 7.43 (s, 5H), 7.3 - 7.04 (m, 5H), 6.84 (dd, J = 1H), 4.27 27 o- (t, J= 6.8 Hz, 2H), 4.16 - 4.09 (m, 7H), 3.16 (t, J=6.8Hz. 2H), 1.04 (t, J=7.1Hz, S 3H) o'0, 8.27 (d, J=2.1Hz, 1H), 7.43 (s, 5H), 7.31 - 6.93 (m, 5H), 6.84 (dd, J=8.4, 2.4 28 b . / Hz, 1H), 4.26 (t, J = 6.9 Hz, 2H), 4.16 - 4.09 (nm, 5H), 3.16 (t, J = 6.9 Hz. 2H), S 1.04 (t, J= 7.0 Hz, 3H) 0, 8.27 (d, J=2.4Hz, 1H), 7.43 (s, 5H), 7.31 - 6.95 (m, 5H), 6.83 (dd, J= 8.4, 2.2 29 F o Hz, 1H), 4.21 (t, J = 6.8 Hz, 2H), 4.14 - 4.09(m, 5H), 3.11 (t, J= 6.8 Hz. 2H), S 1.04 (t, J=7.1Hz, 3H) F F 8.27 (d, J=2.6Hz, 1H), 7.55- 7.44 (m, 9H), 7.15 (d, J= 8.4 Hz, 1H), 6.84 (dd, J 30 = 8.4, 2.4Hz, 1H), 4.29 (t, J=6.6Hz, 2H), 4.18 - 4.03(m, 5H), 3.18 (t, J=6.8Hz, 2H), 1.04 (t, J=7.1Hz, 3H) o 8.37 (d, J= 2.2 Hz, 1H), 8.07 (m, 2H), 7.55 - 7.15 (in, 8H), 6.93 (dd, J = 8.4, 31 2.2 Hz, 1H), 5.12 (s, 2H), 4.28 - 4.03 (m, 5H), 3.92 (s, 3H), 1.05 (t, J = 7.1 Hz, S 3H) o 0 8.27 (d, J=2.4Hz, 1H), 7.69 - 6.90 (m, 12H), 5.57 (t, J=4.5Hz, 1H), 4.19 (s, 32 -\ 3H), 4.05 (t, J=6.3Hz, 2H), 3.22 (t, J=7.2Hz, 1H), 2.82 (t, J=7.1Hz, 2H), 2.14 S (quint, J=6.5Hz, 2H), 0.88 (t, J=7.2Hz, 3H) WO 2005/100303 PCT/KR2005/001066 19 No. structure 1H-NMR (CDCI 3 , 300 MHz) 8 0 8.28 (d, J = 2.6 Hz, 1H), 7.43 (s, 5H), 7.16 (d, J = 8.2 Hz, 1H), 6.86 (dd, J = 33 o / 8.2, 2.6 Hz, 1H), 4.22 -4.09 (m, 7H), 3.74 (t, J = 4.5 Hz, 4H), 2.82 (t, J = 5.6 Hz, 2H), 2.59 (t, J = 4.5 Hz, 4H), 1.04 (t, J = 7.1 Hz, 3H), mp 102-104-C S8.27 (d, J=2.4Hz, 1H), 7.44 (s, 5H), 7.15 (d, J=8.4Hz, 1H), 6.86 (dd, J = 8.4, 34 / 2.4 Hz, 1H), 4.26 (m, 1H), 4.16 - 4.10 (m, 7H), 2.91 (t, J=5.9Hz, 2H1), 2.47 o - 2.40 (m, 4H), 1.92 - 1.72 (m, 8H), 1.70- 1.60 (m, 2H), 1.04 (t, J=7.2Hz, 3H) o0, .- 8.28 (d, J = 2.7 Hz, 1H), 7.41 - 7.14 (m, 4H), 7.05 (d, J = 8.1 Hz, 1H), 6.86 /O D 35 / o-\ (dd, J = 8.1, 2.7 Hz, 1H), 4.17 (s, 3H), 4.13 (q, J = 7.1 Hz, 2H), 3.89 (s, 3H), F 1.01 (t, J = 7.1 Hz, 3H) 0 8.28 (d, J=2.4Hz, 1H), 7.44 (s, 5H), 7.15 (d, 3=8.2Hz, 1H), 6.86 (dd, J = 8.4, 36 Jo- 2.4Hz, 1H), 4.29 - 4.08 (m, 7H), 2.86 (t, J=5.7Hz, 2H), 2.80 - 2.55(m, 8H), 2.34 (s, 3H), 1.05 (t, J=7.2 Hz, 3H) 0, 37 8.30 (m, 1H), 7.36- 7.26 (m, 14H), 3.59 (s, 3H) 3o o 7.68 - 6.85 (m, 13H), 5.40 (d, J=7.8Hz, 1H), 4.19 (s, 3H), 4.03 (t, J=6.3Hz, 38 K 2H), 2.82 (t, J=7.1Hz, 2H), 2.12 (quint, J=6.5Hz, 2H), 0.90 (d, J=6.5Hz, 6H-I), 0 o 7.75 - 6.79 (m, 13H), 5.51 (d, J=7.8Hz, 1H), 4.19 (s, 3H), 4.04 (t, J=6.3Hz, 39 - 2H), 3.77 - 3.73 (m, 1H), 2.82 (t, J=7.1Hz, 2H), 2.13 (quint, J=6.5Hz, 2H), S 1.34- 1.21(m, 10H) o0o 7.82-6.87(m, 13H), 4.11(s, 3H), 4.06(t, J=6.3Hz, 2H), 3.66- 3.26(m, 8H), 40i--o 2.85(t, J=7.1Hz, 2H), 2.16(quint, J=6.5Hz, 2H) WO 2005/100303 PCT/KR2005/001066 20 No. structure 1 H-NMR (CDCI,, 300 MHz) 6 o 7.89 - 6.80 (m, 8H), 4.21 (s, 3H), 4.16 (t, J= 5.4Hz, 2H), 3.86 (m, 1H), 3.75 41 O (t, J=4.8Hz, 4H), 2.83 (t, J=5.4Hz, 2H), 2.60 (t, J=4.8Hz, 4H), 1.63 - 1.18 (m, 10H) o 8.51 (d, J= 8.4 Hz, 1H), 7.45 (s, 5H), 7.29 - 7.14 (m, 5H), 6.88 - 6.80 (nim, 42 2H), 4.27 - 4.11 (m, 5H), 3.96 (t, J = 6.3 Hz, 2H), 2.78 (t, J = 6.3 Hz, 2H), S 2.10 (m, 2H), 1.06 (t, J= 7.1 Hz, 3H) 43f -.. 8.57 (s, 1H), 7.45 - 7.15 (m, 12H), 4.60 (s, 2H), 4.17 - 4.13 (m, 5H), 3.75 S~ 3.63 (m, 2H), 2.99 - 2.84 (m, 2H), 1.25 - 1.10 (m, 3H) 44 8.22 (d, J = 2.5 Hz, 1H), 7.63 - 7.60 (m, 2H), 7.47 - 7.39 (m, 4H), 6.85 (dd, J / = 8.3, 2.5 Hz, 1H), 6.39 (s, 1H), 4.07 (s, 3H), 3.86 (s, 3H) \ o 7.56 - 7.53 (m, 2H), 7.44 -7.41 (m, 3H11), 7.31 (d, J = 8.6 Hz, 1H), 7.12 (d, J = a-n 1.9 Hz, 1H), 6.78 (dd, J= 8.2, 2.2 Hz, 1H), 4.31 -4.11 (m, 7H11), 3.75 (t, J= 45 4.5 Hz, 4H), 2.83 (t, J= 5.6 Hz, 2H), 2.59 (t, J= 4.5 Hz, 4H), 1.24 (t, J = 7.1 Hz, 3H), mnp 151-1521C o. -8.27 (d, J=2.6Hz, 1H), 7.44 (s, 5H), 7.17 (d, J=8.6Hz, 1H), 6.89 (dd, J=8.2, 46 / 2.4Hz, 1H), 4.38 (t, J = 6.2 Hz, 2H), 419 - 4.08 (m, 5H), 3.66 (t, J=6.2Hz, 2H), 1.05 (t, J=7.2Hz, 3H) 0, ., 8.26 (d, J= 2.4 Hz, 1H), 7.33-7.30 (m, 2H11), 7.29-7.27 (m, 4H11), 6.84 (dd, J= 47 8.3, 2.4 Hz, 1H), 4.19 (t, J= 5.5 Hz, 2H), 3.74 (t,J= 4.7 Hz, 4H), 1.39 (s, 9H) 0 48 o 8.18 (s, IH), 7.43 (s, 5H), 6.72 (s, 1H), 6.02 (s, 2H), 4.14 (q, J=7.0Hz, o8 a-\ 2H), 4.12 (s, 3H), 1.04 (t,J=7.0Hz, 3H), mp 119-121'C WO 2005/100303 PCT/KR2005/001066 21 No. structure 'H-NMR (CDCI 3 , 300 MHz) 8 00 0 0 8.26 (s, 1H), 8.06 - 8.00 (m, 2H), 7.52 - 7.14 (m, 9H), 5.17 (s, 2H), 4.18 (s, 49 3H), 4.12- 4.00 (m, 1H), 3.90 (s, 3H), 0.92 (d, J= 6.5 Hz, 6H) o 8.26 (s, 1H), 7.46 - 7.41 (m, 5H), 7.19 - 7.15 (m, IH), 6.87 - 6.81 (m, 1H), 50 o0.) 4.18 - 4.04 (m, 6H), 3.76- 3.71 (m, 4H), 2.85- 2.80 (m, 2H), 2.62- 2.57 (m, 4H), 0.91 (s, 3H), 0.88 (s, 3H), mp 123-125'C 0 8.27 (d, J=2.2 Hz, 1H), 7.50 - 7.40 (m, 5H), 7.18 (d, J=8.2 Hz, 1H), 6.86 (dd, o., ,_< J=8.2, 2.2 Hz, 1H), 5.60 (brs, 1H), 4.19 (s, 3H), 4.18 (t, J=5.6 Hz, 2H), 3.73 (t, 51 J=4.8 Hz, 4H), 2.81 (t, J=5.6 Hz, 2H), 2.73 - 2.65 (m, 1H), 2.58 (t, J=4.8 Hz, 4H), 0.75-0.50 (m, 4H) 0 ,' 8.27 (s, 1H), 7.46 - 6.81 (m, 7H), 5.42 (m, 1H), 4.19 (t, J=5.4Hz, 2H), 3.74 (t, 52 o.. /J=4.8Hz, 4H), 2.83 (t, J=5.4Hz, 2H), 2.59 (t, J=4.8Hz, 4H), 0.97 (s, 3H), 0.94 F (s, 3H) 0 53 ,o 8.66 - 7.00 (m, 8H), 4.17 (s, 3H), 4.15 (q, J=7.2 Hz, 2H), 3.89 (s, 3H), 3.70 (s, 53 / ' T 2H), 1.26 (t, J-7.2 Hz, 3H) 54 o a 7.56 - 6.98 (m, 8H), 4.31 (s, 3H), 4.22 (q, J=7.2 Hz, 2H), 3.87 (s, 3H), 3.68 (s, / 2H), 1.28 (t, J=7.2 Hz, 3H) 8.47 (d, J = 8.0 Hz, 1H), 8.37 (d, J= 2.0 Hz, 1H), 7.50 -7.43 (m, 6H), 7.15 (d, 55 0N o J= 8.1 Hz, 1H), 6.86 - 6.81 (m, 2H), 5.43 (brd, 1H), 4.35 (t, J= 6.6 Hz, 2H), N, 0-() H 4.15 (s, 3H), 4.02 (m, 1H), 3.20 (t, J = 6.6 Hz, 2H), 2.60 (q, J = 7.4 Hz, 2H), 1.24 (t, J = 7.4 Hz, 3H), 0.90 (d, J = 6.7 Hz, 6H) C3 A0 8.27 (s, IH), 7.36-7.16 (m, 10H), 6.85 (dd, J= 8.0, 2.4 Hz, 1H), 4.15 (q, J= 56 / 7.1 Hz, 2H), 4.11 (s, 3H), 4.05 (t, J= 6.2 Hz, 2H), 2.82 (t, J= 7.8 Hz, 2H), 2.42 (s, 3H), 2.05-2.15 (m, 2H), 1.10 (t, J= 7.1 Hz, 3H) WO 2005/100303 PCT/KR2005/001066 22 No. structure 'H-NMR (CDCI 3 , 300 MHz) 6 00 o 8.26 (d, J= 2.4 Hz, 1H), 7.52-7.49 (m, 2H), 7.41 (d, J= 2.4 Hz, 1H), 7.30-7.15 57- (m, 6H), 6.89 (dd, J= 8.4, 2.4 Hz, 1H), 4.28 (q, J= 7.2 Hz, 2H), 4.09 (s, 3H), 57 oN . 4.05 (t, J= 6.0 Hz, 2H), 2.82 (t, J = 7.2 Hz, 2H), 2.15-2.11 (m, 2H), 1.26 (t, J= 7.2, 3H) 0 N 0 8.26 (s, 1H), 7.44-7.09 (m, 10H), 6.82 (dd, J= 8.0, 2.4 Hz, 1H), 4.13 (q, J= 7.4 58 / o Hz, 2H), 4.12 (s, 3H), 4.04 (t, J = 6.2 Hz, 2H), 2.82 (t, J= 7.4 Hz, 2H), 2.15 2.12 (m, 2H), 1.10 (t, J= 7.2 Hz, 3H) Cl 0 0 .o aN- 8.25 (d,J= 2.4 Hz, 1H), 7.47 (d, J= 8.4 Hz, 1H), 6.97 (d, J= 4.0 Hz, 1H), 6.90 59 / o-\ (dd, J= 8.4, 2.8 Hz, 1H), 4.31 (q, J= 7.2 Hz, 1H, 2H), 4.08-4.03 (m, 5H), 2.82 - , (t, J= 7.2 Hz, 2H), 2.15-2.11 (m, 2H), 1.30 (t, J= 7.2 Hz, 3H) 0~ o a 8.26 (d, J= 2.8 Hz, IH), 7.35-7.15 (m, 8H), 7.03 (d, J= 7.6 Hz, 1H), 6.92 (d,J 60 0 = 8.8 Hz, 1H), 6.84 (dd, J= 8.4, 2.8 Hz, 1H), 4.16-4.01 (m, 7H), 2.82 (t, J= 8.0 Hz, 2H), 2.40 (s, 3H), 2.15-2.11 (m, 2H), 1.06 (t, J= 7.6 Hz, 3H) 0, 0 8.27 (d, J= 2.4 Hz, 1H), 7.71-7.70 (m, 1H), 7.54-7.52 (m, 1H), 7.44-6.84 (m, 61 , o 1 4H), 7.30-4.01(m, 7H), 2.82 (t, J= 7.6 Hz, 2H), 2.16-2.09 (m, 2H), 1.43 (t, J= o- 6.8 Hz, 3H) 0 o a 0 8.26 (s, 1H), 7.32-7.15 (m, 6H), 7.00-6.83 (m, 4H), 6.02 (s, 2H), 4.21 (q, J= 62 / - 7.2 Hz, 2H), 4.09 (s, 3H), 4.03 (t, 2H), 2.82 (t, J= 7.2 Hz, 2H), 2.12 (m, 2H), S1.16 (t,J= 7.2 Hz, 3H) 0 a a 8.74-8.72 (m, 1H), 8.20 (d, J= 2.8 Hz, 1H), 7.97 (d, J= 8.4 Hz, 1H), 7.77-7.76 S (m, 2H), 7.31-7.26 (m, 3H), 7.23-7.17 (m, 3H), 6.90 (dd, J= 8.4, 2.4 Hz, 1H), 63 6.86 (s, IH), 4.14 (s, 3H), 4.06 (t, J= 6.4 Hz, 2H), 2.83 (t, J= 8.0 Hz, 2H), 2.10-2.17 (m, 2H) 8.28 (d, J= 2.8 Hz, 1H), 7.74 (d, J= 8.4 Hz, IH), 7.59 (d, J= 1.6 Hz, IH), 64 7.29-7.19 (m, 5H), 7.00 (d, J= 4.0 Hz, 1H), 6.92 (dd, J = 8.4, 2.4 Hz, 1H), 64 N 0 / - 6.69-6.57 (m, 1H), 4.40 (q, J= 7.2 Hz, 2H), 4.08 (s, 3H), 4.05 (t, J = 6.4 Hz, 2H), 2.83 (t, J= 7.6 Hz, 2H), 2.16-2.13 (m, 2H), 1.37 (t, J= 7.2 Hz, 3H) WO 2005/100303 PCT/KR2005/001066 23 No. structure 'H-NMR (CDCI 3 , 300 MHz) 8 0o1. 8.22 (d, J= 2.4 Hz, 1H), 7.30-7.17 (m, 6H), 6.89 (dd, J= 8.4, 2.8 Hz, 1H), 4.37 65 o (q, J= 7.2Hz, 2H), 4.10-4.00 (m, 5H), 2.81 (t, J= 7.2 Hz, 2H), 2.74 (t. J= 7.2 Hz, 2H), 2.15-2.09 (m, 2H), 1.40 (t, J = 7.2 Hz, 3H) 1.24 (t, J= 7.2 Hz, 3H) oi 8.20 (d, J= 2.4 Hz, 1H), 7.30-7.17 (m, 6H), 6.89 (dd, J= 8.0, 2.4 Hz, 1H), 3.97 66 (q, J= 7.2 Hz, 2H), 4.06-4.03 (m, 5H), 2.82 (t. J= 7.2 Hz, 2H), 2.33 (s, 3H), 2.12-2.10 (m, 2H), 1.40 (t, J= 7.2 Hz, 3H) o o 8.26 (d, J= 2.4 Hz, 1H), 7.58 (dd, J= 2.4,1.6 Hz, 1H), 7.42 (m, IH), 7.30-7.26 67 o (m, 4H), 7.23-7.19 (m, 3H), 6.87 (d, J= 2.8 Hz, 1H), 4.22 (q, J= 7.2 Hz, 2H), S 4.07 (s, 3H), 4.05 (t, J= 6.4 Hz, 2H), 2.82 (t, J= 7.6 Hz, 2H), 2.15-2.13 (m, 2H), 1.20 (t, J = 7.2 Hz, 3H) a 8.22 (d, J= 2.4 Hz, IH), 7.31-7.17 (m, 6H), 6.83 (dd, J= 8.4,2.4 Hz, 1H), 4.38 0 ~ 0 68 a (q, J = 7.2 Hz, 2H), 4.02 (t, J= 6.4 Hz, 2H), 4.00 (s, 3H), 2.81 (t, J= 7.8 Hz, 2H), 2.14-2.05 (m, 2H), 1.40 (t,J= 7.2 Hz, 3H), 1.08-1.03 (m, 4H) . 8.27 (d, J= 2.0 Hz, 1H), 7.58-7.57 (m, 1H), 7.43-7.41 (m, 1H), 7.31-7.27 (m, N 69 o /-o- 2H), 6.89 (dd, J= 8.2, 2.0 Hz, 1H), 4.26-4.19 (m, 4H), 4.10 (s, 3H), 3.76-3.74 S (m, 4H), 2.84 (t, J= 5.2 Hz, 2H), 2.61-2.59 (m, 4H), 1.20 (t, J= 7.6 Hz, 3H) S 8.29 (d, J=2.4Hz, 1H), 7.90 (d, J= 8.0 Hz, 1H), 7.62 (d, J= 8.0 Hz, 1H), 7.54 -- /0-xo~ (s, 1H), 7.40-7.30 (m, 2H), 7.28-7.24 (m, 2H), 7.22-7.18 (mn, 3H), 7.05 (d, J= 70 8.4 Hz, 1H), 6.82-6.78 (m, 1H), 4.17 (s, 3H), 4.07-3.97 (m, 4H), 2.82 (t, J= 7.2 Hz, 2H), 2.12 (t, J = 7.2 Hz, 2H), 0.78 (t, J= 7.2 Hz, 3H) ,,o , 8.26 (d, J= 2.4 Hz, 1H), 7.93 (d, J= 8.4 Hz, 1H), 7.54 (d, J= 4.0 Hz, 2H), 71 O 7.29-7.26 (m, 2H), 7.22-7.16 (m, 3H), 6.90 (dd, J= 8.4, 2.4 Hz, 1H), 4.34 (q, J 71 = 7.2 Hz, 2H), 4.05 (s, 3H), 3.77-3.75 (m, 2H), 2.82 (t, J= 7.2 Hz, 2H), 2.14 2.10 (m, 2H), 1.36 (t,J= 7.2 Hz, 3H) 0 -o 8.26 (d, J= 2.4 Hz, 1H), 7.40 (d, J= 8.4 Hz, 1H), 7.31-7.18 (m, 5H), 6.83 (d, J / = 8.4, 2.8 Hz, 1H), 4.36 (q, J= 7.2 Hz, 2H), 4.03 (t, J = 6.2 Hz, 2H), 4.00 (s, 72 3H), 2.81 (t, J= 7.8 Hz, 2H), 2.76-2.68 (m, 1H), 2.15 - 2.08 (m, 2H), 1.85-1.72 (m, 4H), 1.38 (t, J= 7.0 Hz, 3H), 0.85 (t, J= 7.4 Hz, 6H) WO 2005/100303 PCT/KR2005/001066 24 No. structure 1 H-NMR (CDC1 3 , 300 MHz) 8 0 -0 0 8.28 - 6.82 (m, 13H), 5.57 (brs, 2H), 4.23 (s, 3H), 4.05 (t, J=6.0 Hz, 2H11), 73 \NH, S 2.83 (t, J=7.2, 2H), 2.16 - 2.05 (m, 2H) o , 8.25 (s, 1H), 7.49 - 6.84 (m, 12H), 5.39 (d, J= 8.5Hz, 1H), 4.19 (s, 3H), 4.01 74 N-( (m, 1H), 3.96 (d, J=5.3Hz, 2H), 3.92 (d, J=6.5Hz, 2H), 3.75 (t, J= 8.9Hz, S 2H), 3.55 (s, 2H), 2.84 (t, J=8.9Hz, 2H), 0.92 (s, 3H), 0.88 (s, 3H) o 0 8.29 (d, J=2.3Hz, 1H), 7.72 - 7.55 (m, 5H), 7.44 (d, J=8.3Hz, 1H), 7.31 0 75 7.17 (m, 5H), 6.96 (dd, J=8.3, 2.3Hz, 1H), 4.47 (s, 3H), 4.08 (t, J=6.2Hz, 2H), 2.83 (t, J=6.2Hz, 2H), 2.12 (m, 2H), mp 126-128'C (76 a _ 8.08 (s, IH), 7.45 (s, 5H), 6.71 (s, 1H), 5.97 (s, 2H), 5.65 (brs, 1H), 4.15 (s, 76 o o 7 3H), 4.13 - 3.96 (m, 1H), 0.92 (d, J=7.6Hz, 6H) 0 -. 8.55 (s, 1H), 7.45 (s, 5H), 7.44 - 7.15 (m, 3H), 4.17 (q, J= 7.1Hz, 2H), 4.13 77 o o (s, 3H), 3.70 (t, J= 4.8Hz, 4H), 3.57 (s, 2H), 2.46 (t, J= 4.8Hz, 4H), 1.07 (t, S J= 7.1Hz, 3H) 0 0 8.55 (d, J=4.4Hz, 1H), 8.28 (d, 2.3Hz, 1H), 7.53 - 7.43 (n, 4H), 7.34 - 7.26 78 I a (m, 2H), 7.17 - 7.12 (m, 2H), 6.84 (dd, J=8.3Hz, J=2.3Hz, 1H), 4.44 (t, 78 J=6.6Hz, 2H), 4.15 - 4.08 (m, 5H), 3.29 (t, J=6.6Hz, 2H), 1.02 (t, J=7.1Hz, 3H) o0 .- 8.39 (d, J=3.3Hz, 1H), 8.27 (d, J=2.4Hz, 1H), 7.43 (s, 5H), 7.26 (m, 1H), 79 o - 7.21 - 7.11 (m, 2H), 6.86 (d, J=2.4Hz, 1H), 4.43 (t, J=6.5Hz, 2H), 4.39 -4.07 (m, 5H), 3.25 (t, J=6.5Hz, 2H), 2.62 (q, J=7.3Hz, 21H), 1.04 (t, J=6.1Hz, 3H) N, o 8.55 (m, 1H), 8.26 (d, J=2.6Hz, 1H), 7.63 (mn, 1H), 7.49 -7.43 (m, 4H), 7.27 8 0\/ (m, 2H), 7.15 (m, 2H), 6.83 (dd, J=8.3Hz, J=2.6Hz, 1H), 4.43 (t, J=6.7Hz, 80 2H), 4.18 (s, 3H), 3.28 (t, J=6.5Hz, 2H), 0.90 (d, J=5.3Hz, 6H), mp 124 126'C WO 2005/100303 PCT/KR2005/001066 25 No. structure 1 H-NMR (CDCI 3 , 300 MHz) 6 S 8.39 (s, 1H11), 8.25 (d, J=1.8Hz, 1H), 7.47 - 7.45 (mn, 7H), 7.21 - 7.14 (m, 2H), 81 6.82 (dd, J=8.2Hz, J=2.0Hz, 1H), 4.39 (t, J=6.6Hz, 2H), 4.17 (s, 3H), 4.06 (inm, 1H-), 3.25 (t, J=6.25Hz, 2H), 2.63 (q, J=7.4Hz, 2H), 0.90 (d, J=6.5Hz, 311H) a 8.22 (d, J = 2.4 Hz, 1H), 7.64 - 7.35 (m, 6H), 6.88 (dd, J = 8.3, 2.4 Hz, 1H), 82 o) 6.42 (s, 1H), 4.18 (t, J = 6.4 Hz, 2 H), 4.10 (s, 3 H), 3.74 (t, J= 4.5 Hz, 4H), 2.83 (t, J = 5.6 Hz, 2H), 2.59 (t, J= 4.5 Hz, 4H), mp 122-123 1C I -o. o=s9=o o o 8.13 (s, 1H), 7.57-7.30 (m, 5H), 6.85 (s, 1H), 4.21 (q, J= 7.2 Hz, 2H11), 3.92 (s, 83 o83 - ~ 3H), 3.36 (s, 3H11), 3.30 (s, 3H), 1.15 (t, J= 7.2 Hz, 3H) O=s~ 0, 8.26 (d, J = 2.6 Hz, 1H), 7.26-7.23 (m, 5H11), 7.15 (d, J = 8.2 Hz, IH), 6.86 (dd, N 0 S o J = 8.2, 2.6 Hz, 1H1), 4.18 (t, J=5.2 Hz), 4.11 (s, 3H), 3.82 (d, J=6.6Hz, 2H), 84 3.72 (t, J=4.6 Hz, 4H), 2.84 (t, J= 5.2 Hz, 2H), 2.57 (t, J= 4.6 Hz, 4H), 1.65 (sept, J=6.6 Hz), 0.68 (d, J=6.6 Hz, 6H) 0, 85 .. /-- 8.28 - 6.85 (m, 8H), 4.28 - 4.10 (m, 2H), 4.10 (s, 3H), 3.73 (t, J=4.8 Hz, 4H), S 3.66 (s, 3H), 2.82 (t, J-5.4 Hz, 2H), 2.58 (t, J=4.8 Hz, 4H) ot 0, 7.53 - 6.76 (in, 8H11), 4.24 - 4.10 (m, 2H), 4.24 (s, 3H), 3.79 (s, 3H), 3.75 (t, 86 . 0 / J=4.8 Hz, 4H), 2.83 (t, J=5.4 Hz, 2H), 2.59 (t, J=4.8 Hz, 4H) o, 8.28 - 6.82 (m, 8H), 4.20 (t, J=5.6 Hz, 2H11), 4.12 (s, 3H), 4.02 (t, J=6.5 Hz, N0 87 O. a/ __ 2H), 3.74 (t, .J=4.8 Hz, 4H), 2.85 (t, J=5.6 Hz, 2H), 2.61 (t, J=4.8 Hz, 4H), 1.48 - 1.25 (m, 2H), 0.87 (t, J=5.4 Hz, 3H) S 8.27 (d, J= 2.4 Hz, 1H), 7.45-7.42 (m, 2H), 7.17-7.11 (m, 3H), 6.87 (dd, J= 88 oj 8.0, 2.4 Hz, 1H), 4.23-4.12 (m, 7H), 3.77-3.75 (m, 4H), 2.86 (t, J = 5.6 Hz, 2H), 2.65-2.60 (m, 4H11), 1.10 (t, J= 7.2 Hz, 3H) 5F WO 2005/100303 PCT/KR2005/001066 26 No. structure 'H-NMR (CDCI 3 , 300 MHz) 6 S a., 8.61 (d, J= 4.8 Hz, 1H), 8.39 (d, J= 2.4 Hz, 1H), 7.73 (t, J= 7.6 Hz, 1H), 7.55 S(d, J= 7.6, 1H), 7.55 (d, J=7.6, 1H), 7.48-7.21 (m, 6H), 7.17 (d, J= 8.4 Hz, 89 I1H), 6.94 (dd, J= 2.4, 1H), 5.28 (s, 2H), 4.12(s, 3H) 4.12(q, J= 6.8 Hz, 2H), 1.04 (t, J= 6.8 Hz, 3H) o+ 8.41 (s, J= 2.4 Hz, IH), 8.19 (dd, J= 2.0 Hz, 1H), 7.69 (t, 1H), 7.15 (s, 5H), 90 i OE t 7.28 (d, J= 8.4 Hz, 1H), 7.13 (dd, J= 2.0 Hz, 1H), 7.01-6.95 (m, 2H), 4.13 (q, J= 7.2 Hz, 2H), 4.11 (s, 3H), 1.05 (t, J= 7.2 Hz, 3H) 91 o M 0 o 8.38 (s, 1H), 7.44 (s, 5H) 7.28 (t, J= 8.0 Hz, 1H), 7.05-6.91 (m, 4H), 5.13 (s, 91, )_o OEt 2H), 4.12 (s, 3H), 4.13 (q, J= 7.2 Hz, 2H), 1.04 (t, J= 7.2 Hz, 3H) 8.23 (d, J= 2.4 Hz, 1H), 7.59-7.58 (m, 1H), 7.44-7.43 (m, 1H), 7.31-7.27 (m, r92 N o 2H), 6.86 (dd, J= 7.6, 2.4 Hz, 1H), 5.68 (d, J= 8.0 Hz, 1H), 4.18-4.10 (m, ~92 o - 6H), 3.75-3.72 (im, 4H), 2.81 (t, J= 5.6 Hz, 2H), 2.60-2.57 (m, 4H), 1.03 (d, J= 6.4 Hz, 6H) 8.27 (d, J= 2.4 Hz, 1H), 7.41 (d, J= 8.0 Hz, 1H), 6.85 (dd, J = 8.4, 2.8 Hz, a N o 1H), 4.36 (q, J= 7.2 Hz, 2H), 4.18 (t, J= 5.8 Hz, 2H), 4.00 (s, 3H), 3.74 (t. J= 93 0 Et E 4.6 Hz, 4H), 2.82 (t, J= 5.6 Hz, 2H), 2.73-2.68 (m, 1H), 2.58 (t, J = 4.6 Hz, 4H), 1.82-1.75 (in, 4H), 1.39 (t, J= 7.2 Hz, 3H), 0.85 (t, J= 7.2 Hz, 6H) 8.28 (s, J= 2.4 Hz, 1H), 7.92 (d, J= 6.4 Hz, 1H), 7.70 (d, J= 6.4 Hz, IH), , N / o 7.43-7.35 (m, 2H), 7.04 (d, J= 8.8 Hz, 1H), 6.81 (dd, J= 2.4 Hz, 1H) 4.21 (s, 94 0 HN< 3H), 4.17 (t,J= 5.6 Hz, 2H), 3.85 (m, 1H), 3.73 (t, J= 4.4 Hz, 4H), 2.82 (t, J= S 5.6 Hz, 2H), 2.58 (t, J= 4.4 Hz, 4H), 0.74 (d, 3H), 0.59 (d, 3H), mp 77-791C 8.24 (d, J= 2.4 Hz, 1H), 7.51-7.48 (m, 2H), 7.18-7.13 (m, 3H), 6.84 (dd, J= r N--0 7.6, 2.4 Hz, 1H), 5.53 (d, J= 8.0 Hz, IH), 4.19-4.16 (m, 5H), 4.12-4.01 (m, 95o 9/ 1H), 3.75-3.72 (m, 4H), 2.81 (t, J= 5.6 Hz, 2H), 2.59-2.57 (m, 4H), 0.95 (d, J= F 6.4 Hz, 6H) 8.25 (d, J= 2.4 Hz, 1H), 7.33 (d, J= 8.4 Hz, 1H), 6.28 (dd, J= 8.4, 2.4 Hz, 0, 96 N.'OO 1H), 4.27 (m, 1H), 4.17 (t, J= 5.6 Hz, 2H), 4.08 (s, 3H), 3.73 (m, 4H), 2.81 (t, 96 o0 J= 5.6 Hz, 2H), 2.59-2.51 (m, 5H), 1.80 (m, 4H) 1.27 (d, J= 6.4 Hz, 6H), 0.88 (t, J= 7.2 Hz, 6H) WO 2005/100303 PCT/KR2005/001066 27 No. structure 'H-NMR (CDCI, 300 MAHz) 8 S 8.27 (d, J= 2.4 Hz, 1H), 6.89 (s, 2H), 6.82-6.76 (m, 2H), 4.15-4.09 (m, 5H), 97 o0) 01. OEt 4.01 (q, J= 6.8 Hz, 2H), 3.74-3.72 (m, 4H), 2.82 (t, J= 5.6 Hz, 2H), 2.59-2.57 (m, 4H), 2.32 (s, 3H), 2.04 (s, 6H), 1.26 (t, J= 6.8 Hz, 3H) 8.28 (d, J= 2.4 Hz, 1H), 7.20-7.16 (m, 1H), 7.07 (d, J= 7.6 Hz, 2H), 6.83 (dd, /N 0 o J= 7.8, 2.4 Hz, 1H), 6.76 (J= 8.4 Hz, 1H), 4.21-4.17 (m, 5H), 3.99 (q, J= 7.2 98 o / OEL 98 . / 0,Hz, 2H), 3.74-3.72 (m, 4H), 2.82 (t, J= 5.6 Hz, 2H), 2.60-2.57 (m, 4H), 2.09 (s, 6H), 0.81 (t,J= 7.2 Hz, 3H) 8.53 (d, J=4.9 Hz, 1H), 8.48 (d, J = 8.3 Hz, 1H), 7.60 (m, IH), 7.48 - 7.43 (m, -0. , 9 5H), 7.24 - 7.13 (m, 2H), 6.87 - 6.81 (m, 2H), 5.42 (brs, 1H), 4.37 (t, J= 6.6 99 N 0 H Hz, 2H), 4.15 (s, 3H), 4.08 (m, 1H), 3.24 (t, J = 6.6 Hz, 2H), 0.90 (d, J = 6.7 Hz, 6H), mp 158-159"C 8.49 (d, J = 9.0 Hz, 1H), 7.48 - 7.44 (m, 5H), 6.84 - 6.82 (m, 2H), 5.47 (brd, 100 1H), 4.15 (s, 3H), 4.10 (t, J = 5.6 Hz, 2H), 4.05 (m, 1H), 3.71 (t, J = 4.3 Hz, SN H 4H), 2.77 (t, J = 5.6 Hz, 2H), 2.55 (t, J = 4.3 Hz, 4H), 0.90 (d, J = 6.5 Hz, 6H), mp 134-1377C 7.57 - 7.54 (m, 2H), 7.43 - 7.41 (m, 3H), 7.30 (d, 1=8.4Hz, 1H), 7.12 (d, 101 0 0 1 No , J=1.8Hz, 1H), 6.78 (dd, J=8.4, 1.8Hz, 1H), 5.17 (quin, J=6.2Hz, IH), 4.25 (s, 101 0/ 0-K 3H), 4.15 (t, J=5.6Hz, 2H), 3.76 (t, J=4.4Hz, 4H), 2.83 (t, J=5.6Hz, 2H), 2.59 (t, J=4.4Hz, 4H), 1.23 (d, J=6.2Hz, 6H), mp 153-155'C 8.63 (d, J=2Hz, 1H), 8.25 (d, J=2Hz, 1H), 7.63 (m, 1H), 7.40 (m, 1H), 7.29 (m, 1 0 1 N. 112H), 7.15 (m, 1H), 7.19 (m, 3H), 6.87 (m, 1H), 5.44 (d, J=8.5Hz, 1H), 4.46 (t, 102 N 9 S J=6.6Hz, 2H), 4.22 (s, 3H), 4.09 (m, 1H), 3.31 (t, J=6.6Hz, 2H), 0.97 (d, F J=6.6Hz, 6H) 8.40 (d, J=2Hz, 1H), 8.28 (d, J=2Hz, 1H), 7.47 (m, 2H), 7.3 (m, 1H), 7.23 (m, -103 o-. 2H), 7.19 (m, 2H), 6.86 (m, 1H), 5.3 (d, J=7Hz, 1H), 4.43 (t, J=6.6Hz, 2H), 4.2 S (s, 3H), 4.05 (m, 1H), 3.27 (t, J=6.6Hz, 2H), 2.64 (q, J=7.6Hz, 2H), 1.24 (t, F J=7.6Hz, 3H), 0.97 (d, J=6.7Hz, 6H) WO 2005/100303 PCT/KR2005/001066 28 No. structure 'H-NMR (CDCI, 300 MHz) 5 8.28 (d, J= 2.4 Hz, 1H), 7.91 (d, J= 8.0 Hz, 2H), 7.53 (d, J= 8.0 Hz, 2H), 7.10
N
0104 Et (d, J= 8.4 Hz, lH), 6.88 (dd, J= 2.4, 6.0 Hz, 1H), 4.13-4.21 (m, 7H), 3.74 (t, J 104 / OEt S\ = 4.8 Hz, 4H), 2.83 (t, J= 5.6 Hz, 2H), 2.59 (t, J= 4.4 Hz, 4H), 1.07 (t, J=7.2 CN Hz, 3H) 8.55 (d, J = 5.2 Hz, 1H), 8.26 (d, J = 2.4 Hz, 1H), 7.61-7.65 (m, 1H), 7.42 (s, ON 1 o - 0 5H), 7.29 (d, J= 7.6 Hz, 1H), 7.14-7.17 (m, 1H), 7.10 (d,J= 8.4 Hz, 1H), 6.82 S (dd, J= 2.4, 8.4 Hz, 1H), 4.96-5.02 (m, 1H), 4.43 (t, J= 6.4 Hz, 2H), 4.12 (s, 3H), 3.29 (t, J= 6.4 Hz, 2H), 1.04 (d, J=6.4 Hz, 6H) 1) 6-methoxy- l-(trans-methylimino-N-oxy)-3-phenyl- 1lH-indene-2-carboxylate 5 ethyl ester 2) 1-(trans-isopropylimino-N-oxy)-6-methoxy-3-phenyl- 1 H-indene-2 carboxylate ethyl ester 3) 1-(trans-benzylimino-N-oxy)-6-methoxy-3-phenyl-l1H-indene-2-carboxylate ethyl ester 10 4) 1-(trans-ethylimino-N-oxy)-6-methoxy-3-phenyl-1H-indene-2-carboxylate ethyl ester 5) 6-methoxy- 1 -(trans-phenylpropylimino-N-oxy)-3-phenyl- 1H-indene-2 carboxylate ethyl ester 6) 6-methoxy- 1l-(trans-(2-methylbutenylimino)-N-oxy)-3-phenyl- 1 H-indene-2 15 carboxylate ethyl ester 7) 1-(trans-isobutylimino-N-oxy)-6-methoxy-3-phenyl- 1 H-indene-2 carboxylate ethyl ester 8) 1-(trans-methylimino-N-oxy)-6-(2-morphorline-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate ethyl ester 20 9) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 carboxylate ethyl ester WO 2005/100303 PCT/KR2005/001066 29 10) 1-(trans-methylimino-N-oxy)-6-phenetyloxy-3-phenyl- 1H-indene-2 carboxylate ethyl ester 11) 3-furan-3-yl-l-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1IH indene-2-carboxylate ethyl ester 5 12) 6-hydroxy- 1-(trans-methylimino-N-oxy)-3-phenyl- 1H-indene-2 carboxylate ethyl ester 13) 1-(cis-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 carboxylate ethyl ester 14) 3-(trans-methylimino-N-oxy)- 1 -phenyl-3H-indene-5-ol 10 15) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(5-phenylpentyloxy)- 1H-indene 2-carboxylate ethyl ester 16) 1-(cis-methylimino-N-oxy)-3-phenyl-6-(5-phenylpentyloxy)- 1H-indene-2 carboxylate ethyl ester 17) 6-[2-(4-chlorophenoxy)acetoxy]-1 -(trans-methylimino-N-oxy)-3-phenyl 15 1H-indene-2-carboxylate ethyl ester 18) 6-[2-(4-chlorophenoxy)ethoxy]-1 -(trans-methylimino-N-oxy)-3-phenyl- lH indene-2-carboxylate ethyl ester 19) 1-(trans-methylimino-N-oxy)-6-(naphthalene-2-ylmethoxy)-3-phenyl-1H indene-2-carboxylate ethyl ester 20 20) methyl-[3-phenyl-6-(3-phenylpropoxy)indene-1-yllidene] amine-N-oxide 21) 1-(trans-methylimino-N-oxy)-6-[2-(5-methyl-2-phenylthiazol-4-yl)ethoxy] 3-phenyl- 1H-indene-2-carboxylate ethyl ester 22) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)- 1H-indene-2 carboxylate ethyl ester 25 23) 6-[2-(4-hydroxyphenyl)ethoxy]-1l-(trans-methylimino-N-oxy)-3-phenyl-l1H indene-2-carboxylate ethyl ester 24) 6-(2-adaman-1-ylethoxy)- 1-(trans-methylimino-N-oxy)-3-phenyl- 1H indene-2-carboxylate ethyl ester 25) 6-(2-cyclohexylethoxy)- 1-(trans-methylimino-N-oxy)-3-phenyl- 1lH-indene 30 2-carboxylate ethyl ester 26) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylprophenoxy)- 1 H- WO 2005/100303 PCT/KR2005/001066 30 indene-2-carboxylate ethyl ester 27) 6-[2-(2-fluorophenyl)ethoxy]-1-(trans-mnethylimino-N-oxy)-3-phenyl- 1H indene-2-carboxylate ethyl ester 28) 6-[2-(3-fluorophenyl)ethoxy]-l1-(trans-methylimino-N-oxy)-3-phenyl-1H 5 indene-2-carboxylate ethyl ester 29) 6-[2-(4-fluorophenyl)ethoxy]-1-(trans-methylimino-N-oxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 30) 1-(trans-methylimino-N-oxy)-3-phenyl-6-[2-(3 trifluoromethylphenyl)ethoxy]-l1H-indene-2-carboxylate ethyl ester 10 31) 6-(4-methoxycarbonylbenzyloxy)-1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate ethyl ester 32) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)- 1 H-indene-2 carboxylate ethyl amide 33) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1 H 15 indene-2-carboxylate ethyl ester 34) 6-[2-(cyclohexylmethylamino)ethoxy]-1l-(trans-methylimino-N-oxy)-3 phenyl-l1H-indene-2-carboxylate ethyl ester 35) 3-(2-fluorophenyl)-6-methoxy- 1l-(trans-methylimino-N-oxy)- 1 H-indene-2 carboxylate ethyl ester 20 36) 1-(trans-methylimino-N-oxy)-6-[2-(4-methylpiperazine-1-yl)ethoxy]-3 phenyl-l1H-indene-2-carboxylate ethyl ester 37) (2,3-diphenyl indene-1-yl lidene)methylamine-N-oxide 38) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)- 1lH-indene-2 carboxylate isopropyl amide 25 39) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 carboxylate cyclohexyl amide 40) [1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)- 1 H-indene-2 yl]morpholine-4-yl-methanone 41) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-yl-ethoxy)-3-phenyl- 1H 30 indene-2-carboxylate cyclohexyl amide 42) 1-(trans-methylimino-N-oxy)-3-phenyl-5-(3-phenylpropoxy)- 1 H-indene-2- WO 2005/100303 PCT/KR2005/001066 31 carboxylate ethyl ester 43) 1-(trans-methylimino-N-oxy)-6-phenethyloxymethyl-3-phenyl-1H-indene 2-carboxylate ethyl ester 44) (6-methoxy-3-phenylindene-1-yllidene)methylamine-N-oxide 5 45) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-1H indene-2-carboxylate ethyl ester 46) 6-(2-bromoethoxy)- 1 -(trans-methylimino-N-oxy)-3-phenyl- 1H-indene-2 carboxylate ethyl ester 47) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1 H 10 indene-2-carboxylate tert-buthyl ester 48) 1-(trans-methylimino-N-oxy)-5,6-methylenedioxy-l1-oxo-3-phenyl-l1H indene-2-carboxylate ethyl ester 49) 4-[2-isopropylcarbamoyl-3-(trans-methylimino-N-oxy)- 1-phenyl-3H indene-5-yl-oxylmethyl]benzoate methyl ester 15 50) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-1H indene-2-carboxylate isopropyl amide 51) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- lH indene-2-carboxylate cyclopropyl amide 52) 3-(3-fluorophenyl)-l1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 20 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 53) (6-methoxy- 1l-(trans-methylimino-N-oxy)-3-phenyl- 1 H-indene-2-yl)acetate ethyl ester 54) (6-methoxy- 1-(cis-methylimino-N-oxy)-3-phenyl- 1 H-indene-2-yl)acetate ethyl ester 25 55) 5-[2-(5-ethylpyridine-2-yl)ethoxy]- 1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate isopropyl amide 56) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-p-tolyl- 1H-indene-2 carboxylate ethyl ester 57) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-thiophene-2-yl-l1H 30 indene-2-carboxylate ethyl ester 58) 3-(4-chlorophenyl)- 1l-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1 H- WO 2005/100303 PCT/KR2005/001066 32 indene-2-carboxylate ethyl ester 59) 3-(5-chlorothiophene-2-yl)- 1 -(trans-methylimino-N-oxy)-6-(3-phenyl propoxy)-1H-indene-2-carboxylate ethyl ester 60) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-m-tolyl-l1H-indene-2 5 carboxylate ethyl ester 61) 1-(trans-methylimino-N-oxy)-3-(4-phenoxyphenyl)-6-(3-phenylpropoxy) 1H-indene-2-carboxylate ethyl ester 62) 3-benzo-[1,3]-dioxol-5-yl-l1-(trans-methylimino-N-oxy)-6-(3-phenyl propoxy)-l1H-indene-2-carboxylate ethyl ester 10 63) methyl-[6-(3-phenylpropoxy)-3-pyridine-2-yl-indene- 1 -yllidene]-amine-N oxide 64) 3-fuiran-2-yl- 1 -(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1 H indene-2-carboxylate ethyl ester 65) 3-ethyl-I -(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1H-indene-2 15 carboxylate ethyl ester 66) 3-methyl- l-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1H-indene-2 carboxylate ethyl ester 67) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-thiophene-3-yl-lH indene-2-carboxylate ethyl ester 20 68) 3-cyclopropyl-l1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-1H indene-2-carboxylate ethyl ester 69) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-thiophene-3 yl- 1H-indene-2-carboxylate ethyl ester 70) 3-benzo-[b]-thiophene-3-yl-1-(trans-methylimino-N-oxy)-6-(3-phenyl 25 propoxy)-1H-indene-2-carboxylate ethyl ester 71) 3-(1H-imidazole-4-yl)- 1 -(trans-methylimino-N-oxy)-6-(3-phenylpropoxy) 1H-indene-2-carboxylate ethyl ester 72) 3-(1-ethyl propyl)- 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1H indene-2-carboxylate ethyl ester 30 73) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2 carboxylate amide WO 2005/100303 PCT/KR2005/001066 33 74) 6-(4-benzylmorpholine-2-ylmethoxy)- 1-(trans-methylimino-N-oxy)-3 phenyl- 1 H-indene-2-carboxylate isopropyl amide 75) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)- 1lH-indene-2 carbonitrile 5 76) 1-(trans-methylimino-N-oxy)-5,6-methylenedioxy-l1-oxo-3-phenyl-l1H phenyl-2-carboxylate isopropyl amide 77) 1-(trans-methylimino-N-oxy)-6-morpholine-4-ylmethyl-3-phenyl-l1H indene-2-carboxylate ethyl ester 78) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(2-pyridine-2-ylethoxy)-1H 10 indene-2-carboxylate ethyl ester 79) 6-[2-(5-ethylpyridine-2-yl)ethoxy]-1 -(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate ethyl ester 80) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(2-pyridine-2-ylethoxy)-l1H indene-2-carboxylate isopropyl amide 15 81) 6-[2-(5-ethylpyridine-2-yl)ethoxy]-l1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate isopropyl amide 82) methyl-[6-(2-morpholine-4-ylethoxy)-3-phenylindene-1-yllidene]amine-N oxide 83) 5,6-bis-methanesulfonyloxy-1-(trans-methylimino-N-oxy)-3-phenyl-l1H 20 indene-2-carboxylate ethyl ester 84) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1H indene-2-carboxylate isobutyl ester 85) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1H indene-2-carboxylate methyl ester 25 86) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate methyl ester 87) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-1H indene-2-carboxylate propyl ester 88) 3-(4-fluorophenyl)-l1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 30 ylethoxy)-l1H-indene-2-carboxylate ethyl ester 89) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(pyridine-2-ylmethoxy)- 1lH- WO 2005/100303 PCT/KR2005/001066 34 indene-2-carboxylate ethyl ester 90) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(pyridine-2-yloxy)- 1H-indene-2 carboxylate ethyl ester 91) 6-(3-methoxybenzyloxy)- l-(trans-methylimino-N-oxy)-3-phenyl- 1 H 5 indene-2-carboxylate ethyl ester 92) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-thiophene- 3 yl-1lH-indene-2-carboxylate isopropyl amide 93) 3-(1-ethylpropyl)- 1l-(trans-methylimino-N-oxy)-6-(2-morpholine- 4 -yl ethoxy)- 1H-indene-2-carboxylate ethyl ester 10 94) 3-benzo-[b]-thiophene-3-yl-l1-(trans-methylimino-N-oxy)-6-(2-morpholine 4-ylethoxy)-l1H-indene-2-carboxylate isopropyl amide 95) 3-(4-fluorophenyl)- 1l-(trans-methylimino-N-oxy)-6-(2-morpholine-4 ylethoxy)- 1 H-indene-2-carboxylate isopropyl amide 96) 3-(1-ethylpropyl)-l1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 15 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 97) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)- 3
-(
2
,
4
,
6 trimethylphenyl)-l1H-indene-2-carboxylate ethyl ester 98) 3-(2,6-dimethylphenyl)-l1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 ylethoxy)-l1H-indene-2-carboxylate ethyl ester 20 99) 1-(trans-methylimino-N-oxy)-3-phenyl-5-(2-pyridine-2-ylethoxy)-l1H indene-2-carboxylate isopropyl amide 100) 1-(trans-methylimino-N-oxy)-5-(2-morpholine-4-ylethoxy)-3-phenyl- 1H indene-2-carboxylate isopropyl amide 101) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1 H 25 indene-2-carboxylate isopropyl ester 102) 3-(3-fluorophenyl)-l1-(trans-methylimino-N-oxy)-6-(2-pyridine-2 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 103) 6-[2-(5-ethylpyridine-2-yl)ethoxy]-3-(3-fluorophenyl)- 1-(trans methylimino-N-oxy)- 1H-indene-2-carboxylate isopropyl amide 30 104) 3-(4-cyanophenyl)-6-(2-morpholine-4-ylethoxy)- 1-(trans-methylimino-N oxy)-1H-indene-2-carboxylate ethyl ester WO 2005/100303 PCT/KR2005/001066 35 105) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(2-pyridine-2-ylethoxy)-lH indene-2-carboxylate isopropyl ester. The inventive indene derivative of formula (I) and a pharmaceutically 5 acceptable salt thereof is capable of selectively modulating activities of PPARs, and thus it causes no adverse side effects such as weight gain, cardiac hypertrophy, edema and liver damage. The present invention also includes within its scope a pharmaceutical composition comprising a therapeutically effective amount of the novel 10 compounds of formula (I), as defined above, or a pharmaceutically acceptable salt thereof as an active ingredient together with a pharmaceutically acceptable carrier. The inventive pharmaceutical composition is useful for the treatment and prevention of disorders modulated by PPARs, i.e., metabolic syndromes 15 such as diabetes, obesity, arteriosclerosis, hyperlipidemia, hyperinsulinism and hypertension; inflammatory diseases such as osteoporosis, liver cirrhosis and asthma; and cancer. The pharmaceutical compositions of the invention may be formulated for administration orally or parenterally, including intravenous, intraperitoneal, 20 subcutaneous, rectal and topical routes of administration. The composition for oral administration may take various forms such as tablets, soft and hard gelatin capsules, aqueous solutions, suspensions, emulsions, syrups, granules and elixirs, which may contain conventional additives such as a diluent (e.g., lactose, dextrose, sucrose, mannitol, sorbitol, cellulose and glycine), a lubricant (e.g., 25 silica, talc, stearic acid or its magnesium and calcium salts and polyethylene glycol). In the case of the tablet form, the composition may further comprise a binder (e.g., magnesium aluminum silicate, starch paste, gelatin, tragacanth, methyl cellulose, sodium carboxymethyl cellulose and polyvinyl pyrrolidone) and optionally a disintegrant (e.g., starch, agar and alginic acid or its sodium 30 salt), absorbent, colorant, flavor, sweetener and the like. The composition may be sterilized and/or contain an adjuvant such as a preservative, stabilizer, wetting agent, emulsifier, a salt for controlling an osmotic pressure and/or a buffer solution, and other pharmaceutically effective WO 2005/100303 PCT/KR2005/001066 36 materials. The inventive compounds may be administered as an active ingredient in an effective amount ranging from about 0.1 to 500 mg/kg, preferably from about 0.5 to 100 mg/kg per day in a single dose or in divided doses. 5 The following Preparations and Examples are given for the purpose of illustration only and are not intended to limit the scope of the invention. Synthesis of compound of formula ( I) according to reaction scheme (II) 10 Example 1: Preparation of 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3 phenylpropoxy)-1H-indene-2-carboxylate ethyl ester (No. 9 compound of Table 1) 15 (step 1) Preparation of 3-hydroxy benzyl chloride (formula (VI)) 3-Hydroxybenzylalcohol (5 g, 40 mmol) and triethylamine (5.2 mt, 60 nrnnol) were dissolved in benzene (250 mt), and thionylchloride (5.2 mt) dissolved in benzene (50 m) was added thereto at 0 °C. The brownish reacting 20 solution was stirred at room temperature for 6 hours. When the reaction was completed, the solution was washed with brine, and the water layer was extracted with methylene chloride. The organic extract was dried over anhydrous magnesium sulfate and concentrated under a reduced pressure to obtain the title compound (5.7 g, 99 %). 25 'H NMR (CDC1 3 , 200 MHz) 65 7.22 (t, J=7.7 Hz, 1H), 6.96-6.78 (m, 3H), 5.73 (s, 1H), 4.52 (s, 2H) (step 2) Preparation of 2-(3-hydroxybenzyl)-3-oxo-3 30 phenylpropionate ethyl ester (formula VII) Ethyl benzoylacetate (8.7 m0, 50.2 mmol) and potassium carbonate WO 2005/100303 PCT/KR2005/001066 37 (7.56 g, 54.7 mmol) were dissolved in dimethylformamide (500 m0) and stirred at room temperature for 1 hour, and then 3-hydroxybenzyl chloride (6.5 g, 45.6 mmol) dissolved in dimethylformamide (50 m) was added thereto at 0 "C. The brownish reacting solution was stirred at room temperature for 15 hours. 5 When the reaction was completed, the solution was washed with saturated ammonium chloride, and extracted with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate, concentrated under a reduced pressure, and the residue was subjected to silica gel column chromatography (ethyl acetate: hexane=1:5) to obtain the title compound (10.2 g, 75 %) as pale yellow 10 oil. H NMR (CDC1 3 , 200 MHz) 65 7.97-7.92 (m, 2H), 7.56 - 7.39 (m, 3H), 7.11 (t, J= 7.7 Hz, 1H), 6.79 - 6.63 (m, 3H), 5.37 (brs, 1H), 4.62 (t, J= 7.3 Hz, 1H, ), 4.13 (q, J= 7.1 Hz, 2H), 3.27 (d, J= 7.3 Hz, 2H), 1.11 (t, J= 7.1, 3H) 15 (step 3) Preparation of 6-hydroxy-3-phenyl-1H-indene-2 carboxylate ethyl ester (formula (VIM)) 2-(3-Hydroxybenzyl)-3-oxo-3-phenylpropionate ethyl ester (5 g, 16.7 20 mmol) and polyphosphoric acid (20 g) were mixed and stirred at room temperature for 1 hour. The reaction mixture was washed with water to remove polyphosphoric acid, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, concentrated under a reduced pressure. And the residue was subjected to silica gel column 25 chromatography (ethyl acetate: hexane=l1:4) to obtain the title compound (47 %) as yellow sticky oil. 1H NMR (CDC1 3 , 200 MHz) 6 7.44-7.38 (m, 5H), 7.12 (d, J =8.4Hz, 1H), 7.02 (d, J=2.0Hz, 1H), 6.76 (dd, J=8.4, 2.0Hz, 1H), 4.12 (q, J=7.1Hz, 30 2H), 3.80 (s, 2H), 1.12 (t, J=7.1Hz, 3H) WO 2005/100303 PCT/KR2005/001066 38 (step 4) Preparation of 6-hydroxy-1-oxo-3-phenyl-1H-indene-2 carboxylate ethyl ester (formula (II)) 6-Hydroxy-3-phenyl-1H-indene-2-carboxylate ethyl ester (1 g, 3.57 5 mmol) was dissolved in 1,4-dioxane (50 mt), and then selenium dioxide (5.49 g, 53.55 rmmol) was added thereto. The mixture was refluxed for 12 hour with vigorous stirring. The resulting mixture was filtered and concentrated, and the concentrate was extracted with ethyl acetate. The extract was washed with brine, and the organic layer was dried over anhydrous magnesium sulfate, 10 concentrated under a reduced pressure, and the residue was subjected to silica gel column chromatography (ethyl acetate: hexane=1:4) to obtain the title compound (58 %) as a rich red solid. 1 H NMR (CDC1 3 , 200 MHz) 6 7.49 (5H, s), 7.15 (d, J 2.4 Hz, 1H), 15 7.01 (d, J= 7.9 Hz, 1H), 6.91 (dd, J= 8.2, 2.4 Hz, 1H), 4.17 (q, J = 7.1 Hz, 2H), 1.13 (t, J = 7.1, 3H) (Step 5) Preparation of 3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H indene-2-carboxylate ethyl ester [compound of formula (II)] (reaction 20 scheme (VII)) (5-1) 6-Hydroxy-l-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (1.7 g, 25 6.07 mmol), 3-phenylpropanol (1.65 g, 12.14 mmol) and triphenylphosphine (3.18 g, 12.14 mmol) were dissolved in tetrahydrofuran (100 m). Diethyl azodicarboxylate (2 ma, 12.14 mmol) dissolved in tetrahydrofuran (20 m0) was added dropwise thereto at 0 *C. After stirring for 6 hours at room temperature, the mixture was washed with brine, extracted with ethyl acetate, the extract was 30 dried over anhydrous magnesium sulfate, the concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography WO 2005/100303 PCT/KR2005/001066 39 (diethyl ether:hexane = 1:10) to obtain the title compound (yield 85 %) as a dark red solid. 1 H NMR (300MHz, CDC1 3 ): 7.50 (s, 5H), 7.47 - 7.16 (m, 6H), 7.06 (d, J 5 = 8.0 Hz, 1H), 6.80 (dd, J = 8.1, 2.4 Hz, 1H11), 4.18 (q, J = 7.1 Hz, 2H), 4.00 (t, J = 6.2 Hz, 2H), 2.81 (t, J= 7.4 Hz, 1H), 1.15 (t, J= 7.1 Hz, 3H). (5-2) 10 6-Hydroxy-l1-oxo-3-phenyl-l1H-indene-2-carboxylate ethyl ester (2 g, 6.80 mmol), potassium carbonate (1.41 g, 10.194 mmol), and sodium iodide (200 mg, 1.359 mmol) were dissolved in dimethylformamide (100 mt). 1 Bromo-3-phenylpropane (2.01 m0, 13.59 mmol) was added thereto at room temperature, was stirred for 12 hours at 60 0 C, and washed with saturated 15 ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane = 1:4) to obtain the title compound (yield 85 %) as a dark red solid. 20 (Step 6) Preparation of 1-(trans-methyl imino-N-oxy)-6-(3 phenylpropyloxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 9 compound of Table 1] (reaction scheme (I)) 25 (6-1) 3-Phenyl-6-(3-phenylpropyloxy)- 1-oxo- 1H-indene-2-carboxylate ethyl ester (2 g, 4.85 mmol) and hydroxyamine-hydrochloric acid (1.01 g, 14.6 mmol) were dissolved in pyridine (1.57 ml, 19.4 rmmol). The reaction mixture was 30 stirred for 1 hour at 70'C, and washed with saturated ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate WO 2005/100303 PCT/KR2005/001066 40 was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane = 1:2) to obtain 1-hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)- 1H-indene-2 carboxylate ethyl ester (yield 9.5 %) as a yellow solid. 5 1 H-NMR (CDC13, 200 MHz): 8 8.09 (d, J=2.3Hz, 1H), 7.48-7.15 (inm, 11H), 7.10 (d, J=8.4Hz, 1H), 6.86 (dd, J=8.4, 2.3Hz, 1H), 4.16 (q, J=7.1Hz, 2H), 4.04 (t, J =6.3Hz, 2H), 2.83 (t, J =6.3Hz, 2H), 2.10 (min, 2H), 1.04 (t, J =7.1Hz, 3H). 10 1-Hydroxyimino-3-phenyl-6-(3-phenylpropyloxy)-l1H-indene-2 carboxylate ethyl ester (1.98 g, 4.63 mmol), methyl iodide (1.15 ml, 18.5 mmol) and potassium carbonate (1.92 g, 13.9 mmol) were dissolved in dimethylformamide (50 mZ), stirred for 30 min at room temperature, and 15 washed with saturated ammonium chloride. The organic layer obtained by extracting the reaction mixture with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the residue was purified by silica gel column chromatography (ethyl acetate:hexane = 1:2) to obtain the title compound (yield 15 %) as a red solid. 20 (6-2) 1-Oxo-3-phenyl-6-(3-phenylpropoxy)- 1H-indene-2-carboxylate ethyl ester (0.75 g, 1.82 mmol) was dissolved in ethanol (30 im). N-methyl 25 hydroxylamine hydrochloride (0.46 g, 5.4 mmol) and 2,6-lutidine (0.584 g, 5.4 mmol) were added thereto, and stirred for 40 hours at 70 °C in a pressure-tube. Ethanol was removed from the reaction mixture under a reduced pressure, and the resulting residue was extracted with ethyl acetate. After washing with saturated ammonium chloride, the organic layer was dried over anhydrous 30 magnesium sulfate and purified by silica gel column chromatography to obtain the title compound (407 mg, yield 40 %) as a red solid.
WO 2005/100303 PCT/KR2005/001066 41 Example 2: Preparation of 1-(trans-methylimino-N-oxy)-6-(2-morpholine 4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 33 5 compound of Table 1] (Step 1) Preparation of 3-phenyl-6-(2-morpholine-4-ylethoxy)-1-oxo 1H-indene-2-carboxylate ethyl ester [compound of formula (I1)] (reaction scheme (VII)) 10 6-Hydroxy- 1-oxo-3-phenyl- 1H-indene-2-carboxylate ethyl ester [compound of formula (1)] (10.90 g, 26.75 mmol) prepared in Step 4 of Example 1 was dissolved in tetrahydrofuran:benzene (270 mt:90 m). Then, 4-(2-hydroxyethyl)morpholine (5.83 g, 44.45 mmol) and triphenylphosphine 15 (11.66 g, 44.45 mmol) were added thereto. Diisopropylazodicarboxylate (8.99 g, 44.45 mmol) was added dropwise to the mixture at 0OC, and stirred for 2 hours at room temperature. The reaction mixture was washed with saturated sodium chloride and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was 20 purified by column chromatography (ethyl acetate) to obtain the title compound (14 g, yield 93 %) as a red solid. 1H NMR (200MHz, CDCl 3 ): 8 7.50 (s, 5H), 7.19 (d, J=2.0 Hz, 1H), 7.07 (d, J=8.2 Hz, 1H), 6.84 (dd, J=8.2, 2.2 Hz, 1H11), 4.22-4.14 (min, 4H), 3.73 (t: 25 J=4.5 Hz, 4H), 2.81 (t, J=5.6 Hz, 2H), 2.57 (t, J=4.5 Hz, 4H), 1.15 (t, J=7.1 Hz, 3H). (Step 2) Preparation of 1-(trans-methylimino-N-oxy)-6-(2 morpholine-4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 30 33 compound of Table 1] (reaction scheme ( I)) WO 2005/100303 PCT/KR2005/001066 42 3-Phenyl-6-(2-morpholine-4-ylethoxy)- 1 -oxo- 1H-indene-2-carboxylate ethyl ester (14.6g, 35.83mmol) was dissolved in ethanol. N-methyl hydroxylamine hydrochloride (8.98 g, 107.49 mmol) and 2,6-lutidine (11.52 g, 107.49 mmol) were added thereto and the mixture was stirred for 3 days at 70 0 C 5 in a pressure-tube. Ethanol was removed under a reduced pressure and the resulting residue was extracted with ethyl acetate. After washing with saturated ammonium chloride, the organic layer was dried over anhydrous magnesium sulfate and purified by column chromatography to obtain the title compound (4.18 g, yield 27 %, mnp 102-104'C) as a red solid. 10 Example 3: Preparation of 1-(trans-methylimino-N-oxy)-5,6 methylenedioxy-1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 48 compound of Table 1] 15 (Step 1) Preparation of 5-chloromethylbenzo[1,3]dioxol [compound of chemical formula (VI)] Piperonyl alcohol (10 g, 65.7 mmol) was dissolved in benzene. 20 Triethylamine (11 rm, 78.8 mmol) and thionyl chloride (11 mk, 131.4 mmol) were added dropwise thereto and was stirred for 24 hours at 0 °C. The reaction mixture was extracted with sodium bicarbonate and ethyl acetate, the organic layer was separated, and dried over anhydrous magnesium sulfate to obtain 5 chloromethyl benzo[1,3]dioxol (11.2 g, yield 100 %). 25 1H NMR (200MHz, CDCl 3 ): 8 6.88-6.75 (min, 3H), 5.97 (s, 2H), 4.53 (s, 2H). (Step 2) Preparation of 2-benzo[1,3]dioxol-5-ylmethyl-3-oxo-3 30 phenylpropionate ethyl ester [compound of formula (VII)] WO 2005/100303 PCT/KR2005/001066 43 5-Chloromethyl benzo[1,3]dioxol (11.2 g, 65.7 mmol) was dissolved in Dimethylformamide. Then, potassium carbonate (18.2 g, 131.4 mmol), sodium iodide (10.8 g, 72.27 mmol) and ethyl benzoylacetate (12.5 ml, 72.27 mmol) were added thereto and stirred for 5 hours at room temperature. The 5 reaction mixture was extracted with ammonium chloride and ether, the organic layer was separated, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 2 benzo[1,3]dioxol-5-ylmethyl-3-oxo-3-phenylpropionate ethyl ester (16.4 g, 76%). 10 1 H NMR (200MHz, CDC1 3 ): 6 7.98-6.69 (m, 3H), 5.90 (s, 2H), 4.56 (t, J=7.4 Hz, 1H), 4.09 (q, J=7.2 Hz, 2H), 3.26 (d, J=7.4 Hz, 2H), 1.13 (t, J=7.2 Hz, 3H). 15 (Step 3) Preparation of 5,6-methylenedioxy-3-phenyl-1H-indene-2 carboxylate ethyl ester [compound of formula (VIl)] 2-Benzo[1,3]dioxol-5-ylmethyl-3-oxo-3-phenylpropionate ethyl ester (16 g, 49.03 mmol) and polyphosphoric acid (160 g) were mixed and stirred for 20 1 hour at room temperature. After the reaction was completed, the mixture was washed with water to remove polyphosphoric acid, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 5,6-methylenedioxy-3-phenyl-1H-indene-2-carboxylate ethyl ester 25 (4.53 g, yield 30 %) as a white solid. 1 H NMR (200MHz, CDC1 3 ): 8 7.41 (m, 5H), 7.00 (s, 1H), 6.69 (s, 1H), 5.96 (s, 2H), 4.08 (q, J=7.2 Hz, 2H), 3.75 (s, 2H), 1.10 (t, J=7.2 Hz, 3H). 30 (Step 4) Preparation of 5,6-methylene dioxy-1-oxo-3-phenyl-1H indene-2-carboxylate ethyl ester [compound of formula (II)] WO 2005/100303 PCT/KR2005/001066 44 5,6-Methylenedioxy-3-phenyl-l1H-indene-2-carboxylate ethyl ester (3 g, 9.73 mmol) was dissolved in 1,4-dioxane. Selenium dioxide (10.8 g, 97.3 rmmol) was added thereto and the reaction mixture was refluxed while stirring 5 for 1 day, followed by cooling. The solution obtained after filtering residual solid selenium dioxide was combined with 1M sodium bicarbonate, and extracted with ether/water. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 5,6-methylenedioxy-l1-oxo-3-phenyl-l1H-indene-2 10 carboxylate ethyl ester (2.18 g, yield 70 %). 1H NMR (200MHz, CDC1 3 ): 6 7.51 (s, 5H), 7.11 (s, 1H), 6.67 (s, 1H), 6.07 (s, 2H), 4.17 (q, J=7.2 Hz, 2H), 1.17 (t, J=7.2 Hz, 3H). 15 (Step 5) Preparation of 1-(trans-methylimino-N-oxy)-5,6-methylene dioxy-1-oxo-3-phenyl-lH-indene-2-carboxylate ethyl ester [No. 48 compound of Table 1] (reaction scheme ( I )) 5,6-Methylenedioxy- 1-oxo-3-phenyl- I H-indene-2-carboxylate ethyl 20 ester (100 mg, 0.324 mmol) was dissolved in ethanol. 2,6-Lutidine (0.11 mi, 0.973 mmol) and methyl hydroxyl amine (81.27 mg, 0.973 mmol) were added thereto and the mixture was stirred for 3 days at 70 °C in a pressure-tube. The reaction mixture was extracted with saturated sodium chloride and ethyl acetate, the organic layer was separated, dried over anhydrous magnesium sulfate, 25 concentrated, and the resulting residue was purified by column chromatography (10~20 % ethyl acetate/hexane) to obtain 1-(trans-methylimino-N-oxy)-5,6 methylenedioxy-l1-oxo-3-phenyl-l1H-indene-2-carboxylate ethyl ester (10 mg, yield 9 %, mp 119-121 "C). 30 Preparation of compound of chemical formula (I) according to WO 2005/100303 PCT/KR2005/001066 45 reaction scheme (III) Example 4: Preparation of 1-(trans-methylimino-N-oxy)-6-(2 morpholine-4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate isopropyl amide 5 [No. 50 compound of Table 1] (Step 1) Preparation of 1-(3-benzyloxyphenyl)ethanone 3-Hydroxyacetophenone (136.15 g, 1 mol), potassium carbonate 10 (414.63 g, 2 mol), KI (33.2 g, 0.2 mol), and benzyl bromide (171.04 g, 1 mol) were dissolved in acetone and the reaction mixture was refluxed while stirring for 24 hours, followed by washing with brine. The reaction mixture was extracted with ethyl acetate, the extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column 15 chromatography (ethyl acetate:hexane = 1:3) to obtain 1-(3-benzyloxyphenyl) ethanone (221.8 g, yield 98 %) in an oil state. 'H NMR (200MHz, CDC1 3 ): 6 7.59-7.53 (m, 2H), 7.44-7.33 (m, 6H) 7.19 (m, 1H), 5.11 (s, 2H), 2.6 (s, 3H). 20 (Step 2) Preparation of 3-(3-benzyloxyphenyl)-3-oxo-propionate ethyl ester [compound of formula (IX)] 1-(3-Benzyloxyphenyl)ethanone (218 g, 966.10 mmol) was dissolved in 25 diethyl carbonate and sodium hydride (60 % oil) (46.37 g, 1.15 mmol) was slowly added thereto at 0 C, and then stirred for 3 hours at 60 °C. After the reaction was completed, ice water and acetic acid were added to the reaction mixture, extracted with ethyl acetate/saturated sodium chloride, the organic layer was separated, and dried over anhydrous magnesium sulfate. The 30 solvent was removed under a reduced pressure and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:10) to obtain 3-(3- WO 2005/100303 PCT/KR2005/001066 46 benzyloxyphenyl)-3-oxopropionate ethyl ester (184.68 g, yield 84 %) in an oil state. 1H NMR (200MHz, CDC1 3 ): 8 7.59-7.50 (m, 2H), 7.47-7.32 (m, 6H), 5 7.21 (m, 1H), 5.11 (s, 2H), 4.29-4.16 (m, 2H), 3.97 (s, 2H), 1.37-1.23 (m, 3H). (Step 3) Preparation of 2-(3-benzyloxybenzoyl)-N-isopropyl-3 phenylacryl amide [compound of formula (IX)] 10 3-(3-Benzyloxyphenyl)-3-oxopropionate ethyl ester (174.42 g, 584.47 mmol) was dissolved in m-xylene and the reaction mixture was refluxed while stirring for 30 min at 150 0 C. Then, isopropylamine (38 g, 642.92 mmol) was added dropwise to the mixture. After stirring and refluxing for 24 hours at room temperature, the organic layer was extracted with saturated sodium 15 chloride and ethyl acetate, dried over anhydrous magnesium sulfate, concentrated, and resulting residue was purified by column chromatography (ethyl acetate:hexane= 1:2) to obtain 2-(3-benzyloxybenzoyl)-N-isopropyl-3 phenylacryl amide (127.13 g, yield 70 %) as yellow oil. 20 1H NMR (300MHz, CDC1 3 ): 5 7.60-7.58 (m, 2H), 7.43-7.34 (m, 5H11), 7.26-7.21 (m, 2H), 6.62 (b, 1H1), 5.10 (s, 2H), 4.11 (m, 1H11), 3.89 (s, 2H), 1.26 1.17 (m, 6H). (Step 4) Preparation of 2-(3-benzyloxybenzoyl)-N-isopropyl-3 25 phenylacryl amide [compound of formula (XI)] 3-(3-Benzyloxyphenyl)-N-isopropyl-3-oxopropionamide (115.75 g, 371.744 mmol) was dissolved in benzene. Then, benzaldehyde [compound of formula (X)] (39.45 g, 371.74 mmol), piperidine (6.33 g, 74.34 mmol), and 30 acetic acid (11.16 g, 185.87 mmol) were added thereto. The mixture was stirred and refluxed for 3 hours. After washing with saturated sodium chloride WO 2005/100303 PCT/KR2005/001066 47 /sodium bicarbonate, the organic layer was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, concentrated, recrystallized, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:20) to obtain 2-(3-benzyl oxy benzoyl)-N-isopropyl-3-phenyl 5 acryl amide (107.74 g, yield 73 %) as a white solid. 1H NMR (300MHz, CDC1 3 ): 8 8.14 (s, 1H), 7.49-7.35 (m, 8H), 7.19 7.12 (m, 5H), 6.62 (b, 1H), 5.00 (s, 2H), 4.17 (m, 1H), 1.18 (d, J=6.6Hz, 6H). 10 (Step 5) Preparation of 5-hydroxy-3-oxo-l-phenylindane-2 carboxylate isopropyl amide [compound of formula (XII)] 2-(3-Benzyloxybenzoyl)-N-isopropyl-3-phenylacryl amide (106.74 g, 267.19 mmol) was dissolved in dichloromethane. Methanesulfonic acid 15 (256.78 g, 2.672 mmol) was added thereto and the mixture was stirred for 3 hours at room temperature. After the reaction was completed, the mixture was cooled to 0 C followed by adding saturated sodium bicarbonate, and the organic layer extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was 20 purified by column chromatography (ethyl acetate:hexane=l1:2) to obtain 5 hydroxy-3-oxo- 1-phenylindane-2-carboxylate isopropyl amide (36.086 g, yield 44 %) as a white solid. 'H NMR (300MHz, CDC1 3 ): 8 7.33-7.10 (m, 7H), 6.71 (d, J=7.8Hz, 1H), 25 5.74 (b, 1H11), 5.16 (d, J=3.9Hz, 1H), 4.10 (m, 1H), 3.41 (d, J=3.9Hz, 1H), 1.28 1.16 (m, 6H). (Step 6) Preparation of 6-hydroxy-1-oxo-3-phenyl-1H-indene-2 carboxylate isopropyl amide [compound of formula (I)] 30 Phenylselenylchloride (15.53 g, 81.07 mmol) was dissolved in WO 2005/100303 PCT/KR2005/001066 48 dichloromethane and the temperature was adjusted to O'C. Pyridine (7.00 g, 88.44 mmol) was added thereto. After 20 min, 5-hydroxy-3-oxo-l-phenyl indane-2-carboxylate isopropyl amide (22.8 g, 73.70 mmol) dissolved in dichloromethane was slowly added to the reaction mixture, which was further 5 stirred for 3 hours. After the reaction was completed, the resultant was combined with 2N-hydrochloric acid and excess 30 % hydrogen peroxide at 0 IC . After adding water and saturated sodium bicarbonate to the mixture, the organic layer was extracted with dichloromethane, dried over anhydrous magnesium sulfate, concentrated, recrystallized, and filtered (ethyl 10 acetate:hexane=1:2) to obtain 6-hydroxy- 1 -oxo-3-phenyl-l1H-indene-2 carboxylate isopropyl amide (16.32 g, yield 72 %) as a red solid. 1H NMR (300MHz, CDC1 3 +DMSO-d 6 ): 8 9.76 (b, 1H), 7.76 (d, J=7.8Hz, 1H), 7.56-7.44 (min, 4H), 6.88 (d, J=8.1Hz, 1H), 6.76 (dd, J=8.1Hz, 15 J=2.1Hz, 1H), 4.11 (m, 1H), 1.18 (d, J=6.3Hz, 6H). (Step 7) Preparation of 6-(2-morpholine-4-ylethoxy)-1-oxo-3-phenyl 1H-indene-2-carboxylate isopropyl amide [compound of formula (II)] (reaction scheme (VI1)) 20 6-Hydroxy-l1-oxo-.3-phenyl-lH-indene-2-carboxylate isopropyl amide (7.0 g, 22.78 mmol) was dissolved in tetrahydrofuran:benzene (150 m:50 Mt). Then, hydroxyethylmorpholine (3.59 g, 27.33 mmol) and triphenyl phosphine (7.17 g, 27.33 mmol) were added thereto. When the temperature was adjusted 25 to 0OC, diisopropyl azodicarboxylate (5.53 g, 27.33 mmol) was added dropwise to the mixture followed by stirring for 2 hours at room temperature. The mixture was washed with brine and extracted with ethyl acetate. The separated organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography 30 to obtain 6-(2-morpholine-4-yl ethoxy)- 1-oxo-3-phenyl- 1H-indene-2 carboxylate isopropyl amide (9.5 g, yield 99 %).
WO 2005/100303 PCT/KR2005/001066 49 1 H NMR (300MHz, CDC1 3 ): 8 7.8 (m, 1H), 7.57-7.47 (m, 4H), 7.12 (d, J=2.4Hz, 1H), 6.98 (d, J=8.1Hz, 1H), 6.79 (dd, J=8.1Hz, J=2.4Hz, 1H), 4.18 (t, J=5.4Hz, 2H), 3.74 (t, J=4.5Hz, 4H), 2.81 (t, J=5.4Hz, 2H), 2.57 (t, J=4.5Hz, 5 4H), 1.19 (d, J=6.6Hz, 6H). (Step 8) Preparation of 1-(trans-methylimino-N-oxy)-6-(2 morpholine-4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate isopropyl amide [No. 50 compound of Table 1] (reaction scheme ( I)) 10 6-(2-Morpholine-4-ylethoxy)- 1 -oxo-3-phenyl- 1H-indene-2-carboxylate isopropyl amide (9.30 g, 22.11 mmol) was dissolved in ethanol. N-methyl hydroxylamine hydrochloride (5.54 g, 66.35 mmol) and 2,6-lutidine (7.11 g, 66.35 mmol) were added thereto and the mixture was stirred for 3 days at 75 0 C 15 in a pressure reactor. After removed ethanol under reduced pressure, the resultant was washed with saturated sodium chloride. Then, the organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by gel column chromatography to obtain 1-(trans-methyl imino-N-oxy)-6-(2-morpholine-4 20 ylethoxy)-3-phenyl-1H-indene-2-carboxylate isopropyl amide (3.8 g, yield 38 %). Preparation of compound of formula (I) according to reaction scheme 25 (IV) Example 5: Preparation of 1-(trans-methylimino-N-oxy)-6-(3 phenylpropyloxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 9 compound of Table 1] 30 (Step 1) Preparation of 3'-(3-phenylpropyloxy)acetophenone WO 2005/100303 PCT/KR2005/001066 50 [compound of formula (IX)] 3'-Hydroxyacetophenone (6.81 g, 50 rmmol) and 1-bromo-3-phenyl propane (11.95 g, 60 mmol) were dissolved in dimethylformamide (70 mi). 5 Then, potassium carbonate (15 g) and sodium iodide (0.5 g) were added thereto and the mixture was allowed to react for 7 hours at 80'C. Ethyl acetate (300 mt) and purified water (200 m) were further added to the reaction mixture prior to stirring for 30 min. The organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was 10 purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to obtain the title compound (12.0 g, yield 94.2 %) as a gel. 1 H-NMR (200MHz, CDCl 3 ): 8 7.47-7.55 (2H11, min), 7.36 (1H11, t, J = 8.0 Hz), 7.27-7.30 (2H11, min), 7.18-7.22 (3H11, min), 7.13 (1H, dd, J= 9.2, 2.8 Hz), 4.01 15 (2H, t, J= 6.2 Hz), 2.82 (2H, t, J= 8.0 Hz), 2.59 (3H, s), 2.13 (2H, min). (Step 2) Preparation of 3'-(3-phenylpropyloxy)benzoylacetate ethyl ester [compound of formula (IX)] 20 3'-(3-Phenylpropyloxy)acetophenone (12.7 g, 50 mmol) obtained in (Step 1) of Example 5 and diethyl carbonate (7.1 g, 60 mmol) were dissolved in toluene (120 m). While maintaining a temperature of 80-90 0 C, sodium hydride (2.6 g) was added dropwise thereto. At the same temperature, the reaction mixture was reacted for 2 hours followed by neutralizing with acetic 25 acid. The organic layer extracted with purified water (200 m0) and ethyl acetate (200 m) was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:8) to obtain the title compound (8.4 g, yield 51.5 %) as a gel. 30 1 H-NMR (200MHz, CDC1 3 ): 5 7.47-7.55 (2H, min), 7.36 (1H, t, J= 8.0 WO 2005/100303 PCT/KR2005/001066 51 Hz), 7.27-7.30 (2H, m), 7.18-7.22 (3H, m), 7.13 (1H, dd, J= 9.2, 2.8 Hz), 4.22 (2H, q, J= 7.2 Hz), 4.01 (2H, t, J= 6.2 Hz), 2.82 (2H, t, J= 8.0 Hz), 2.13 (2H, m), 1.26(3H, t, J= 7.2 Hz). 5 (Step 3) Preparation of 2-benzoyl-3-{3'-(3-phenylpropyloxy) phenyl}-3-oxo-propionate ethyl ester [compound of chemical formula (XIV)] 3'-(3-Phenylpropyloxy)benzoylacetate ethyl ester (8.2 g, 25.2 mmol) 10 obtained in (Step 2) of Example 5 and sodium hydride (1.1 g, 27.7 mmol) were added to methylene chloride (150 ml) and the reaction mixture was stirred for 1 hour at room temperature. Then, benzoyl chloride (3.65 g, 26.0 mmol) was added thereto and the mixture was further stirred for 2 hours at room temperature. The resultant was washed with purified water (200 m), 15 dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:8) to obtain the title compound (7.4 g, yield 68.5 %) as a gel. 20 (Step 4) Preparation of 3-phenyl-6-(3-phenylpropyloxy)-1-oxo-1H indene-2-carboxylate ethyl ester [compound of formula (II)] 2-Benzoyl-3- {3'-(3-phenylpropyloxy)phenyl}-3-oxo-propionate ethyl ester (6.4 g, 14.8 mmol) obtained in (Step 3) of Example 5 and methane 25 sulfonic acid (15 g) were dissolved in methylene chloride (150 mt) and the mixture was stirred for 2 hours at room temperature. Then, additional methylene chloride (150 mg) and saturated ammonium chloride (200 m) were added thereto and the mixture was further stirred for 30 min. The extracted methylene chloride layer was dried over anhydrous magnesium sulfate, 30 concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to obtain the title compound (3.4 g, WO 2005/100303 PCT/KR2005/001066 52 yield 55.5 %) as a gel. 1 H-NMR (200MHz, CDC1 3 ): 6 7.51 (5H, s), 7.17-7.29 (6H, min), 7.06 (1H, d, J= 8.1 Hz), 6.80 (1H, dd, J= 8.1, 2.4 Hz), 4.18 (2H, q, J = 7.1 Hz), 4.01 5 (2H, t, J= 6.3 Hz), 2.81 (2H, t, J= 7.3 Hz), 2.12-2.16 (2H, in), 1.16 (3H, t, J= 7.1 Hz). (Step 5) Preparation of 1-(trans-methylimino-N-oxy)-6-(3-phenyl propyoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 9 compound 10 of Table (IX)] (reaction scheme ( I)) 3-Phenyl-6-(3-phenylpropyloxy)- 1-oxo- 1H-indene-2-carboxylate ethyl ester (2.0 g) obtained in (Step 4) of Example 5 and N-methylhydroxyl amine.hydrochloric acid (2.0 g) were dissolved in ethanol (30 m). 2,6 15 Lutidine (2.4 g) was added thereto and the mixture was stirred for 60 hours. Then, the reaction mixture was concentrated, extracted with water (100 mat) and ethyl acetate (100 mt), washed three times with water. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:4) to 20 obtain the title compound (120 mg, yield 5.6 %, mp 95-97 'C) as a gel. Preparation of compound of formula 1 according to reaction scheme (V) 25 Example 6: Preparation of 1-(tranis-methylimino-N-oxy)-3-phenyl-6-(3 phenylpropoxy)-1H-indene-2-carbonitrile [No. 75 compound of Table 1] (Step 1) Preparation of 3-phenyl-6-(3-phenylpropoxy)indene-1 one[compound of formula (XV)] 30 3-Phenyl-l1-[3-(3-phenylpropoxy)phenyl]propenone (20 g, 58.406 WO 2005/100303 PCT/KR2005/001066 53 mmol) and polyphosphonic acid (200 g) were mixed and stirred for 6 hours at 45 0 C. The mixture was washed with water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl 5 acetate:hexane=1:5) to obtain 3-phenyl-6-(3-phenylpropoxy)indane- 1-one (17.9 g, yield 81 %) as a white solid. 1H NMR (300MHz, CDC1 3 ): 8 7.36-7.09 (min, 13H), 4.52 (dd, J =7.8, 3.6Hz, 1H), 4.01 (t, J =6.3Hz, 2H), 3.25 (dd, J =19.3, 7.7Hz, 1H), 2.81 (t, J 10 =7.1Hz, 2H), 2.68 (dd, J=19.3, 3.6Hz, 1H), 2.14 (m, 2H). (Step 2) Preparation of 2-bromo-3-phenyl-6-(3-phenylpropoxy) indane-1-one [compound of formula (XVI)] 15 3-Phenyl-6-(3-phenylpropoxy)indene-l-one (200 mg, 0.586 mmol) way dissolved in carbon tetrachloride, and N-bromosuccinimide (313 rmg, 1.75 mmol) and 2,2'-azobisisobutyronitrile (9.7 mg) were added thereto. Then, the mixture was refluxed for 1 hour under a 375 W tungsten lamp. After the reaction was completed, saturated sodium chloride was added thereto and 20 extracted with dichloromethane. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=1:5) to obtain title compound (147 mg, yield 60 %) as a red solid. 25 1 H NMR (300MHz, CDC1 3 ): 8 7.69-7.16 (m, 11H), 7.02 (d, J=8.2Hz, 1H), 6.74 (dd, J=8.2, 2.3Hz, 1H), 3.97 (t, J=6.4Hz, 2H), 2.81 (t, J=6.3Hz, 2H), 2.11 (min, 2H). (Step 3) Preparation of 1-oxo-3-phenyl-6-(3-phenylpropoxy)-1H 30 indene-2-carbonitrile [compound of formula (1)] WO 2005/100303 PCT/KR2005/001066 54 2-Bromo-3-phenyl-6-(3-phenylpropoxy)indene-1 -one (1.0 g, 2.3 mmol) was dissolved in N,N-dimethylformamide (10 mt). Copper (I) cyanide (617 mg, 6.9 mmol) was added thereto and the mixture was stirred for 3 hours at 150 0 C. The mixture was cooled, and saturated ammonium chloride was 5 added thereto. The organic layer was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane = 1:3) to obtain the title compound (700 mg, yield 80 %) as a red solid. 10 1H NMR (200MHz, CDC1 3 ): 5 7.83-7.18 (m, 12H), 6.89 (dd, J =8.2, J =2.3Hz, 1H), 4.02 (t, J=6.5Hz, 2H), 2.81 (t, J=6.3Hz, 2H), 2.13 (m, 2H). (Step 4) Preparation of 1-hydroxyimino-3-phenyl-6-(3-phenyl propoxy)-1H-indene-2-carbonitrile (cis, trans compound) [compound of 15 formula (III)] (reaction scheme (I)) 1-Oxo-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2-carbonitrile (200 mg, 0.547 mmol) was dissolved in ethanol. Hydroxy amine-hydrochloric acid (114 mng, 1.64 mmol) and pyridine (173 mrg, 2.18 mmol) were added thereto and the 20 mixture was stirred for 4 hours at 70 0 C. The organic layer extracted with ethyl acetate was washed with distilled water, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane = 1:2) to obtain trans 1-hydroxy imino 3-pheniyl-6-(3-phenylpropyloxy)-1H-indene-2-carbonitrile (95 mg, yield 45 %) 25 as a red solid, 'H NMR (300MHz, CDCl 3 ): 8 9.21 (brs, 1H), 7.94 (d, J =2.3Hz, 1H), 7.74-7.71 (min, 2H11), 7.56-7.54 (min, 3H), 7.43 (d, J =8.4Hz, 1H), 7.32-7.20 (m, 5H), 6.96 (dd, J=8.4, 2.3Hz, 1H), 4.05 (t, J=6.3Hz, 2H), 2.83 (t, J=6.3Hz, 2H11), 30 2.14 (min, 2H); WO 2005/100303 PCT/KR2005/001066 55 and cis -isomer (5 mg, yield 2 %) as a yellow solid. 'H NMR (300MHz, CDC1 3 ): 8 9.71 (brs, 1H11), 7.96 (d, J =2.3Hz, 1H), 7.74-7.71 (m, 2H), 7.56-7.54 (m, 3H), 7.43 (d, J =8.3Hz, 1H), 7.36-7.20 (m, 5 5H), 6.94 (dd, J=8.3, 2.3Hz, 1H), 4.03 (t, J=6.3Hz, 2H), 2.81 (t, J=6.3Hz, 2H), 2.13 (m, 2H). (Step 5) Preparation of 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3 phenylpropoxy)-1H-indene-2-carbonitirile [No. 75 compound of Table 1] 10 (reaction scheme ( I)) Trans- 1 -hydroxyimino-3-phenyl-6-(3-phenylpropoxy)- 1H-indene-2 carbonitile (90 mg, 0.23 mmol) was dissolved in N,N-dimethylformamide. Methyl iodide (134 mg, 0.94 mmol) and potassium carbonate (98 mg, 0.71 15 mmol) were added thereto and the mixture was stirred for 10 min at room temperature. After the reaction was completed, the reaction mixture was cooled, and saturated ammonium chloride was added thereto. The organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography 20 (ethyl acetate:hexane = 1:2) to obtain the title compound (11 mg, yield 12 %) as a red solid, 1H NMR (300MHz, CDCl 3 ): 8 8.29 (d, J =2.3Hz, 1H), 7.72-7.55 (m, 5H), 7.44 (d, J=8.3Hz, 1H), 7.31-7.17 (m, 5H), 6.96 (dd, J =8.3, 2.3Hz, 1H), 25 4.47 (s, 3H), 4.08 (t, J=6.2Hz, 2H), 2.83 (t, J=6.2Hz, 2H), 2.12 (m, 2H11); and trans- 1-methoxyimino-3-phenyl-6-(3-phenylpropoxy)- 1H-indene-2 carbonitrile (69 mg, yield 74 %). 30 Preparation of compound of formula (I) according to reaction scheme WO 2005/100303 PCT/KR2005/001066 56 Example 7: Preparation of 1-(trans-methylimino-N-oxy)-6-(morpholine-4 ylmethyl)-3-phenyl-1H-indene-2-carboxylic ethyl ester [No. 77 compound 5 of Table 1] (Step 1) Preparation of 3-oxo-3-m-tolylpropionate ethyl ester Sodium hydride (3.1 g, 77.1 mmol) and diethyl carbonate were 10 combined with 3-methylacetophenone (4.5 g, 33.54 mmol). The mixture was stirred for 2 hours at 80 0 C. After the reaction was completed, ice water and acetic acid were added thereto. Then, the mixture was extracted with ethyl acetate/saturated sodium chloride. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by 15 column chromatography to obtain 3-oxo-3-m-tolylpropionate ethyl ester (5.8 g, yield 84 %). 1H NMR (200MHz, CDC1 3 ): 8 7.83-7.63 (m, 2H), 7.42-7.28 (min, 2H), 4.27-4.18 (m, 2H), 3.97 (s, 2H), 2.40 (s, 3H), 1.36-1.23 (m, 3H). 20 (Step 2) Preparation of 2-(3-methyl benzoyl)-3-phenylacrylate ethyl ester 3-Oxo-3-m-tolylpropionate ethyl ester (1 g, 4.84 mmol) was dissolved 25 in benzene, and benzaldehyde (0.51 g, 4.84 mmol), acetic acid (0.15 g, 2.49 mmol) and piperidine (0.06 g, 0.8 mmol) were added thereto. The mixture was refluxed for 4 hours. After the reaction was completed, the organic layer extracted with ethyl acetate/saturated sodium chloride/sodium bicarbonate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue 30 was purified by column chromatography to obtain 2-(3-methylbenzoyl)-3 phenylacrylate ethyl ester (1 g, yield 70 %).
WO 2005/100303 PCT/KR2005/001066 57 'H NMR (200MHz, CDC1 3 ): 8 7.98 (s, 1H), 7.86-7.73 (m, 2H), 7.35 7.21 (m, 7H), 4.26-4.19 (m, 2H), 2.39 (s, 3H), 1.20-1.16 (m, 3H). 5 (Step 3) Preparation of 5-methyl-3-oxo-1-phenylindane-2 carboxylate ethyl ester 2-(3-Methylbenzoyl)-3-phenylacrylate ethyl ester (1 g, 3.39 mmol) was dissolved in dichloromethane. Methanesulfonic acid (5.22 g, 54.35 mmol) 10 was added thereto and the mixture was stirred for 3 hours at room temperature. After the reaction was completed, the mixture was cooled to 0oC followed by neutralizing with sodium bicarbonate. Then, the separated organic layer extracted with dichloromethane was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography 15 (ethyl acetate:hexane=1:9) to obtain 5-methyl-3-oxo-l1-phenyl-indene-2 carboxylate ethyl ester (273 mg, yield 27 %). 111 NMR (200MHz, CDCl 3 ): 5 7.73-7.61 (m, 1H), 7.48-7.04 (m, 7H), 4.98-4.94 (m, 1H11), 4.29-4.22 (m, 2H), 3.67-3.60 (m, 1H), 2.41 (s, 3H) 1.33-1.13 20 (m, 3H). (Step 4) Preparation of 6-methyl-l-oxo-3-phenyl-1H-indene-2 carboxylate ethyl ester 25 Phenylselenyl chloride (72 mg, 0.37 mmol) was dissolved in dichloromethane. The mixture was cooled to 0 0 C, combined with pyridine (32 mg, 1.2 mmol), and stirred for about 20 min. The mixture containing 5 methyl-3-oxo-l-phenylindane-2-carboxyl acid ethyl ester (100 mg, 0.34 mmol) dissolved in methane was further added followed by stirring for 2 hours at room 30 temperature. After the reaction was completed, 10 % hydrochloric acid (5 mi) was added into the mixture prior to cooling to 0 0 C. After adding 30 % WO 2005/100303 PCT/KR2005/001066 58 hydrogen peroxide (1 mt) and water (5 m), the separated organic layer extracted with dichloromethane was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane=l1:7) to obtain 6-methyl-l-oxo-3-phenyl-l1H-indene-2 5 carboxylate ethyl ester (51 mg, yield 51 %). 1H NMR (200MHz, CDC1 3 ): 8 7.51-7.04 (min, 8H), 4.24-4.12 (min, 2H), 2.39 (s, 3H), 1.25-1.12 (min, 3H). 10 (Step 5) Preparation of 6-bromomethyl-1-oxo-3-phenyl-1H-indene 2-carboxylate ethyl ester [compound of formula (XIX)] 6-Methyl-l1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (3 g, 10.3 mmol) was dissolved in carbon tetrachloride, and N-bromosuccinimide (2 15 g, 11.4 mmol) and 2,2'-azobisisobutyronitrile (500 mng, 3.09 mmol) were added thereto. Then, the mixture was refluxed for 3 hours under a 375 W tungsten lamp. After the reaction is completed, the organic layer was extracted with dichloromethane/saturated sodium chloride, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column 20 chromatography to obtain 6-bromomethyl-l1-oxo-3-phenyl-l1H-indene-2 carboxylate ethyl ester (1.4 g, yield 36.7 %) as yellow oil. 1 H NMR (200MHz, CDC1 3 ): 6 7.79-7.16 (min, 8H), 4.50 (s, 2H), 4.26 (q, J= 7.1Hz, 2H), 1.16 (t, J= 7.1Hz, 3H). 25 (Step 6) Preparation of 6-(morpholine-4-ylmethyl)-1-oxo-3-phenyl 1H-indene-2-carboxylate ethyl ester [compound of formula (XIX)] 6-Bromomethyl-l1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester 30 (1.1 g, 2.96 mmol) was dissolved in N,N-dimethylformamide. Pyridine (264 !l, 3.26 mmol) and morpholine (284 [1l, 3.26 mmol) were added thereto and the WO 2005/100303 PCT/KR2005/001066 59 mixture was stirred for 2 hours. After the reaction was completed, the organic layer was extracted with ethyl acetate/ammonium chloride/saturated sodium chloride, dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 180 mg of 5 6-(morpholine-4-yl methyl)-l1-oxo-3-phenyl-1H-indene-2-carboxylate ethyl ester (180 mg, yield 16.1 %) as red oil. 1H NMR (200MHz, CDC1 3 ): 8 7.61-7.11 (min, 8H), 4.19 (q, J= 7.1Hz, 2H), 3.70 (t, J=4.8Hz, 4H), 3.51 (s, 2H), 2.44 (t, J=4.8Hz, 4H), 1.15 (t, 10 J= 7.1Hz, 3H). (Step 7) Preparation of 1-(trans-methylimino-N-oxy)-6-(morpholine 4-ylmethyl)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 77 compound of Table 1] (reaction scheme ( I)) 15 6-(Morpholine-4-ylmethyl)- 1 -oxo-3-phenyl- 1 H-indene-2-carboxylate ethyl ester (110 mg, 0.29 mmol) was dissolved in N-methylhydroxyl amine.hydrochloride (73 mng, 0.87 mmol), and 2,6-lutidine (34 pl, 0.87 mmol) were added thereto. The mixture was reacted for 3 days at 70 0 C. After the 20 reaction was completed, ethanol was half concentrated, and the organic layer was extracted with ethyl acetate/saturated sodium chloride. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain 1-(trans-methylimino-N oxy)-6-(morpholine-4-ylmethyl)-3-phenyl-l1H-indene-2-carboxylate ethyl ester 25 (5.3 mg, yield 4.5 %). Preparation of compound of chemical formula ( I) according to reaction scheme (II) 30 Example 8: Preparation of 1-(trans-methylimino-N-oxy)-6-(3-phenyl-propyl WO 2005/100303 PCT/KR2005/001066 60 oxy)-3-phenyl-1H-indene-2-carboxylate cyclohexyl amide [No. 39 compound of Table 1] (Step 1) Preparation of 3-phenyl-6-(3-phenylpropyloxy)-1-oxo-lH 5 indene-2-carboxylate methyl ester 3-Phenyl-6-(3-phenylpropyloxy)- 1-oxo- 1H-indene-2-earboxylate ethyl ester (1.65 g, 4.0 mmol) prepared in (Step 5) of Example 1 was dissolved in methanol (160 mt) and p-toluene sulfonic acid (228 mg, 1.2 mmol) was added 10 thereto. The mixture was reacted for 1 hour at 70 0 C, and then washed with brine. The organic layer was extracted with ethyl acetate, dried over anhydrous sulfonate sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate: hexane=1:9) to obtain the title compound (yield 75.3 %) as a red solid. 15 1H NMR (200MHz, CDC1 3 ): 6 7.43 (s, 5H), 7.27-6.77 (min, 7H), 3.92 (t, J=6.3Hz, 2H), 3.65 (s, 3H11), 2.73 (t, J=7.1Hz, 2H), 2.03 (p, J=6.5Hz, 2H). (Step 2) Preparation of 3-phenyl-6-(3-phenylpropyloxy)--oxo-1H 20 indene-2-carboxylate Tribromoborone-dimethyl sulfide complex (1.94 m£, 9.03 mmol) was suspended in 1,2-dichloroethane (15 mt), and 3-phenyl-6-(3-phenylpropyloxy) 1-oxo-1H-indene-2-carboxylate methyl ester (1.2 g, 3.0 mmol) dissolved in 1,2 25 dichloroethane (10 mt) was added thereto. The mixture was stirred for 2 hours at 90oC followed by cooling to room temperature. After adding sodium bicarbonate, the resulting solution was acidified to pH 2.0 with 6N-hydrochloric acid solution, and then washed with brine. The organic layer was extracted with dichloromethane, dried over anhydrous sulfonate sulfate, concentrated, and 30 the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=3:7-5:5) to obtain the title compound (yield 75.3 %) as a red WO 2005/100303 PCT/KR2005/001066 61 solid. 1H NMR (200MHz, CDCl 3 ): 6 7.69-6.82 (m, 13H), 4.03 (t, J=6.3Hz, 2H), 2.83 (t, J=7.1Hz, 2H), 2.14 (p, J=6.5Hz, 2H); 5 EI-MS m/z (relative intensity): 381 (M-3, 6.92), 148 (7.91), 117 (6.47), 64 (7.69), 44 (100). (Step 3) Preparation of 3-phenyl-6-(3-phenylpropyloxy)-1-oxo-lH indene-2-carboxylate cyclohexylamide 10 3-Phenyl-6-(3-phenylpropyloxy)- 1-oxo- 1H-indene-2-carboxylate (200 mg, 0.52 mmol) was dissolved in dichloromethane (10 mt). Triethylamine (240 l, 1.72 rmmol) and cyclohexylamine (59 pl, 0.52 mmol) were added thereto at 10 C. Then, after adding bis(2-oxo-3-oxazolidinyl)phosphinic 15 chloride (137 mg, 0.52 mmol), the reaction mixture was stirred for about 20 min at room temperature followed by additional 1 hour at 10 0 C. After the water was added thereto to complete the reaction, pH was adjusted to 1-1.5 with 4N hydrochloric acid. The mixture was washed with brine, and extracted with dichloromethane. The extract was dried over anhydrous sulfonate sulfate, 20 concentrated, and the resulting residue was purified by column chromatography (ethyl acetate:hexane
=
1:9~2:8) to obtain the title compound (yield 59.8 %) as a red solid. 1 H NMR (200MHz, CDC13): 6 7.68-6.80 (m, 13H), 3.98 (t, J=6.3Hz, 25 2H), 3.87 (m, 1H), 2.81 (t, J=7.1Hz, 2H), 2.11 (p, J=6.5Hz, 2H1), 1.80-1.20 (m, 10H); EI-MS m/z (relative intensity): 467 (M
+
, 4.81), 382 (14.64), 248 (53.46), 164 (13.54), 90 (100). 30 (Step 4) Preparation of 1-(trans-methylimino-N-oxy)-6-(3 phenylpropyloxy)-3-phenyl-1H-indene-2-carboxylate cyclohexyl amide [No.
WO 2005/100303 PCT/KR2005/001066 62 39 compound of Table 1] (reaction scheme (I)) 3-Phenyl-6-(3-phenylpropyloxy)- 1 -oxo- 1H-indene-2-carboxylate cyclohexylamide (50 mg, 0.11 mmol) was dissolved in ethanol and N-methyl 5 hydroxyl amine.hydrochloride (27 mg, 0.33 mmol), and 2,6-lutidine (38 p1, 0.33 mmol) were added thereto. The mixture was reacted for 3 days at 70 0 C. After the reaction was completed, ethanol was half concentrated, and the organic layer was extracted with ethyl acetate/saturated sodium chloride. The extract was dried over anhydrous magnesium sulfate, concentrated, and the 10 resulting residue was purified by column chromatography to obtain 1-(trans methyl imino-N-oxy)-6-(3-phenylpropyloxy)-3-phenyl- 1H-indene-2 carboxylate cyclohexyl amide (13.1 mg, yield 24 %) as a red solid. 15 Example 9: Preparation of 1-(trans-methylimino-N-oxy)-3-phenyl-5-(2 pyridine-2-ylethoxy)-1H-indene-2-carboxylate isopropyl amide [No. 99 compound of Table 1] (Step 1) Preparation of acetate 2-isopropyl carbamoyl-l1-oxo-3phenyl 20 1H-indene-5-yl ester Phenylselenyl chloride (5.4 g, 28.2 mmol) was dissolved in dichloromethane (CH 2 Cl 2 , 100 mt). The mixture was cooled with ice water, and pyridine (2.45 g, 31 mmol) was added dropwise thereto followed by stirring 25 for about 20 min while maintaining the temperature. 2-Isopropyl carbamoyl-1 oxo-3-phenyl indene-5-yl ester acetate (9.0 g, 25.6 mmol) dissolved in dichloromethane (150 m) was added dropwise thereto and the mixture was stirred for 3 hours at room temperature. After the reaction was completed, 2N hydrochloric acid was added into the mixture prior to cooling to 0 0 C. After 30 adding excess 30 % hydrogen peroxide (H 2 0 2 ) and sodium bicarbonate, the separated organic layer was extracted with dichloromethane and concentrated.
WO 2005/100303 PCT/KR2005/001066 63 The resulting solid residue was dissolved in excess ethyl acetate (300 mk), and washed with diluted hydrochloric acid. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was recrystallized in ethyl acetate to obtain the title compound (7.6 g, yield 85 %) as a yellow solid. 5 1 H NMR (300MHz, CDC1 3 ): 8 7.74 (brd, J = 7.5 Hz, 1H), 7.57 - 7.48 (m, 6H), 7.08 (dd, J = 7.8, 1.8 Hz, 1H), 6.83 (d, J = 1.8 Hz, 1H11), 4.16 (m, 1H), 2.27 (s, 3H), 1.20 (d, J = 6.6 Hz, 6H) Mass spectrum m/e (relative intensity): 349 (M , 3), 291 (3), 249 (6), 10 163 (8), 58 (48), 43 (100). (Step 2) Preparation of 5-hydroxy-1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate isopropyl amide 15 2-Isopropylcarbamoyl- 1-oxo-3phenyl- 1H-indene-5-yl ester acetate (6.26 g, 17.9 mmol) was dissolved in ethanol (200 mt). N-methylhydroxylamine hydrochloride (4.52 g, 53.7 mmol) and 2,6-lutidine (5.75 g, 53.7 mmol) were added thereto and the mixture was stirred for 40 hours at 75'C in a pressure reactor. Ethanol was removed under reduced pressure, and the resulting 20 residue was extracted with ethyl acetate. After washing with diluted hydrochloric acid solution, the organic layer was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column chromatography to obtain the title compound (3.1 g, yield 51 %). 25 1 H NMR (300MHz, DMSO-d 6 ): 5 9.91 (s, 1H), 8.54 (d, J=7.9 Hz, 1H), 8.29 (d, J = 8.1 Hz, 1H), 7.50-7.43 (m, 5H), 6.72-6.69 (m, 2H), 4.01 (s, 3H), 3.89 (m, 1H), 0.93 (d, J = 6.6 Hz, 6H). (Step 3) Preparation of 1-(trans-methylimino-N-oxy)-3-phenyl-5-(2 30 pyridine-2-ylethoxy)-1H-indene-2-carboxylate isopropyl amide WO 2005/100303 PCT/KR2005/001066 64 5-Hydroxy- 1 -(trans-methylimino-N-oxy)-3-phenyl- 1H-indene-2 carboxylate isopropyl amide (3.77 g, 11.2 mmol) was dissolved in tetrahydrofuran:benzene (300 m:100 m0). Then, 2-(2-pyridyl)ethanol (1.93 g, 15.7 mmol) and triphenylphosphine (4.13 g, 15.57 mmol) were added thereto. 5 Diisopropyl azodicarboxylate (3.14 g, 15.7 mmol) was added dropwise to the mixture followed by stirring for 2 hours at room temperature when thd temperature was adjusted to 0 0 C. The mixture was washed with brine and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by column 10 chromatography to obtain the title compound (3.36 g, yield 68 %) as a yellow solid. Isomer transformation between cis and trans 15 Example 10: Transformation of 1-(trans-methylimino-N-oxy)-6-(2 morpholine-4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester [No. 33 compound of Table 1] to cis-isomer 20 (10-1) Base reaction 50 mg of 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3 phenyl- 1H-indene-2-carboxylate ethyl ester was dissolved in tetrahydrofuran:methanol (10 m:10 mt) and 3 equivalents of lithium 25 hydroxide was added thereto. After reacting for 2 days at room temperature, the concentrated mixture was washed with saturated sodium chloride and extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, the concentrated, and the resulting residue was purified by column chromatography to obtain 1-(cis-methylimino-N-oxy)-6-(2-morpholine 30 4-ylethoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester (yield 10 %).
WO 2005/100303 PCT/KR2005/001066 65 (10-2) Photochemical reaction 50 mg of 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3 phenyl-1H-indene-2-carboxylate ethyl ester was dissolved in ethanol (30 m) 5 and excess lithium chloride was added thereto, followed by subjecting the UV irradiation at 250 nm. After reacting for 12 hours, the solution was analyzed by HPLC to determine that 25 % of 1-(cis-methylimino-N-oxy)-6-(2 morpholine-4-ylethoxy)-3-phenyl-l1H-indene-2-carboxylate ethyl ester was produced. 10 Formulation Example 1: Preparation of syrup A syrup containing the hydrochloride of the compound of Example 2 15 was prepared using the ingredients shown in Table 2 by dissolving hydrochloride of 1-(methyl imino-N-oxy)-6-(2-morpholine-4-yl ethoxy)-3 phenyl-1H-indene-2-carboxylate ethyl ester, saccharine, and sugar in warm water, cooling, and adding other ingredients thereto to a volume of 100 m. 20 Table 2 Ingredients Content Hydrochloride of 1-(methylimino-N-oxy)-6-(2-morpholine- 2 2g 4-yl-ethoxy)-3-phenyl-l1H-indene-2-carboxylate ethyl ester Saccharine 0.8 g Sugar 25.4 g Glycerin 8.0 g Flavoring 0.04 g Ethanol 4.0 g Sorbic Acid 0.4 g Distilled Water Fixed amount WO 2005/100303 PCT/KR2005/001066 66 Formulation Example 2: Preparation of a tablet A tablet containing the hydrochloride of the compound of Example 2 5 was prepared with the ingredients shown in Table 3 by mixing hydrochloride of 1-(methylimino-N-oxy)-6-(2-morpholine-4-yl-ethoxy)-3-phenyl- 1 H-indene-2 carboxylate ethyl ester with lactose, potato starch and colloidal silica and adding a 10 % gelatin solution thereto. Then the mixture was crushed, sieved4 through a 14 mesh and dried. Finally the remaining ingredients were added 10 thereto and tableting was performed. Table 3 Ingredients Content Hydrochloride of 1-(methylimino-N-oxy)-6-(2-morpholine- 250 g 250 g 4-yl-ethoxy)-3-phenyl- 1H-indene-2-carboxylate ethyl ester Lactose 175.9 g Potato Starch 180 g Colloidal Silica 32 g 10% gelatin Solution 25g Potato Starch 160 g Talc 50 g Magneisum Stearate 5 g 15 Formulation Example 3: Preparation of an injection liquid The hydrochloride of 1-(methylimino-N-oxy)-6-(2-morpholine-4-yl ethoxy)-3-phenyl-1H-indene-2-carboxylate ethyl ester, sodium chloride and ascorbic acid were dissolved in distilled water in amounts as shown in Table 4 20 and sterilized.
WO 2005/100303 PCT/KR2005/001066 67 Table 4 Ingredients Content Hydrochloride of 1-(methylimino-N-oxy)-6-(2-morpholine-4-yl- 1 1g ethoxy)-3-phenyl-lH-indene-2-carboxylate ethyl ester Sodium Chloride 0.6 g Ascorbic Acid 0.1 g Distilled Water Fixed amount Test Example 1: PPARy activation test 5 The activity for PPARy activation was examined as follows. The vector fused with the ligand binding domain of a human PPARy gene and the DNA binding site of a yeast GAL-4 gene, and luciferase reporter vector were simultaneously transfected in NIH/3T3 cell. The cells were cultured for 24hrs. The solution containing the cells at a concentration of 2x10 4 cells/well 10 was placed on a 96-well plate. Then, each of the test compounds of the present invention or the control group without test compounds was added thereto. After incubating for 24hrs, the cells were subjected to lysis. The luciferase activity of the resultant was then measured, and the activation activity of the test compound was expressed as EC 50 (the concentration at which 50% of 15 the maximum activation was observed) to compute the activation intensities of the test compounds and the comparative compound, rosiglitazone, relative to PPARy. The results are shown in Table 5. Rosiglitazone having the formula (XX) was prepared according to the method described in J. Med. Chem. 1994, 37, 3997.
WO 2005/100303 PCT/KR2005/001066 68 Table 5 No. of Compound of Table 1 ECso (nlM) 8 25 9 40 10 200 11 40 13 150 15 150 25 50 33 15 34 70 36 28 38 170 39 45 41 12 42 80 43 80 45 15 48 10 50 200 68 10 73 110 75 95 77 170 78 15 79 20 80 100 81 45 94 80 Rosiglitazone 320 WO 2005/100303 PCT/KR2005/001066 69 0 N N O SNH I 0 (XX) As shown in Table 5, the inventive compounds exhibited superior 5 PPARy activation activities over the comparative compound, rosiglitazone. Test Example 2: Effectiveness in lowering blood glucose level 10 The effectiveness in lowering blood glucose levels of the inventive compound was examined using ob/ob mice (male, 8-9 weeks old), a type 2 diabetes model animal which expresses signs of hyperglycemia and hyperinsulinemia, and bred at in-house facilities of Korea Research Institute of Chemical Technology. 15 The hydrochloric acid salt of 1-hydroxy-6-(2-morpholine-4-yl-ethoxy) 1,3-diphenyl-lH-indene-2-carbo-xylic acid ethyl ester prepared in Example 8 was suspended in saline/0.2% Tween 80. The resulting solution was intraperitoneally administered to the mice at a dose of 50 mg/kg, once a day for 5 days, or orally administered to the mice, at a dose of 100 mg/kg, twice a day 20 for 14 days. Days 1, 3 and 5 were selected for intraperitoneal administration, and days 5, 10 and 14, for oral administration, to collect blood samples for measuring the blood glucose levels. The extent of inhibition of the inventive compound relative to the control (saline-0.2% Tween 80 in the absence of the compound) is shown in Table 6. Upon the completion of the oral 25 administration for 14 days, the mice were fasted for 16 brs to perform OGTT(Oral Glucose Tolerance Test) to determine the changes in insulin sensitivity induced by the oral administration. After administrating glucose to the mice at a dose of 2g/kg orally, blood samples were collected at 0, 15, 30 60 WO 2005/100303 PCT/KR2005/001066 70 and 120 minutes to measure blood glucose levels. The change in the total amount of blood glucose was computed over the 120-minute period to assess the extent of enhancing glucose clearance rates by compound treatment. The results are shown in Table 6, as % inhibition of total amount of blood glucose 5 by the compound treatment relative to the untreated group. Table 6 Classification % Inhibition 10 Intraperitoneal Administration (50 mg/kg/day) 32.0 Oral Administration (100 mg/kg/day) 23.7 Oral Glucose Tolerance Test (Blood Glucose) 10.2 Moreover, C57/BL6J mice (male, 4 weeks old) which received high fat 15 diet (60% fat) for 10-11 weeks and showed hyperglycemia and insulin resistance were chosen to carry out similar experiments (oral administration for 14 days but once a day) as described above. The extents of suppression of blood glucose and insulin levels were measured as mentioned above. The results are shown in Table 7. To check possible adverse side effects caused by 20 the administration of the compound, the weight, heart weight and liver weight of each mouse were measured. GPT and GOT values were also calculated by employing a kit available in the market. The results are listed in Table 8. Table 7 Classification % Inhibition (%) Blood glucose concentration 30.0 Blood insulin concentration 44.6 Oral Glucose Tolerance Test 23.8 (Glucose)/56.2 (Insulin) 25 WO 2005/100303 PCT/KR2005/001066 71 Table 8 Weight Heart Weight Liver Weight GPT / GOT (g) (g) (g) (karmen) Standard 38 ± 2.8 0.142 ± 0.006 1.56 ± 0.13 91 32/67 ± 17 (High fat diet) Compound of the psn ivn 35 ± 1.1 0.123 ± 0.007 1.06 ± 0.17 29 3.2 / 39 ± 7.8 present invention Rosiglitazone 39 ± 1.6 0.140 ± 0.009 1.56 ± 0.18 85 ± 12 / 70 ± 8.2 As shown in Tables 6, 7, and 8, the inventive compound has an excellent effect in lowering both blood glucose and insulin levels, when it is administered 5 by either orally or intraperitoneally with no side effects such as weight gain, hepatotoxicity or cardiotoxicity. While the invention has been described with respect to the above 10 specific embodiments, it should be recognized that various modifications and changes may be made to the invention by those sldkilled in the art which also fall within the scope of the invention as defined by the appended claims.

Claims (13)

1. An indene derivative of formula (I) or a pharmaceutically acceptable salt thereof: O" R7 'I N +, ,j R, R6 RR2 5R R4 R3 (I) wherein, R 1 is C 1 - 6 alkyl, C1- 6 alkenyl or C 3 - 6 cycloalkyl, which is unsubstituted or substitutied with one or more phenyl groups; O 10 R 2 is H, CN, CO 2 Ra, CH 2 CO 2 Ra, CONRR R, or phenyl; O 0 N R 3 is C1- 6 alkyl, C 3 6 cycloalkyl, or naphthyl, phenyl, , , or H , which is unsubstituted or substitutied with one or more substituents selected from the group consisting of halogen, CN, NH 2 , NO 2 , ORa, phenyloxy, C 1 -6 alkyl and C 3 - 6 cycloalkyl; and 15 R 4 , R 5 , R 6 and R 7 are each independently H, OH, OSO 2 CH 3 , O(CH 2 )mRe, CH 2 R', OCOCH2OR g, OCH2CH20R' or OCH2CH=CHR g, or Rs and R 6 together form OCH 2 0; in which Ra is H, or C1-6 alkyl or C 3 - 6 cycloalkyl, which is unsubstituted or substitutied with one or more halogens; 20 R b and Rc are each independently H, C 1 -6 alkyl or C 3 - 6 cycloalkyl; WO 2005/100303 PCT/KR2005/001066 73 Rd is O, S or NRa; Re is H, halogen, C 3 - 6 cycloalkyl, naphthyl, , , , , or phenyl, which is, unsubstituted or substituted with one or more substituents selected from the 5 group consisting of halogen, CN, NH 2 , NO 2 , ORa, CF 3 and COOR"; - -N Rd R f is OCH2CHR g or , R9 is phenyl, which is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, CN, NH 2 , NO 2 and ORa; and 10 m is an integer in the range of 1 to 5.
2. The compound of claim 1, wherein R 1 is C 1 - 6 alkyl, which is unsubstituted or substitutied with a phenyl group; R 2 is H, CN, CO 2 Ra, CH 2 CO 2 Ra, CONRbR c or phenyl; R 3 is C1- 6 alkyl, C 3 - 6 cycloalkyl, or phenyl, 'k> o~iI N 0 S SN 15 , , , , or H , which is unsubstituted or substitutied with one or more substituents selected from the group consisting of halogen, C 1 - 6 alkyl and C 3 - 6 cycloalkyl; R 4 and R 7 are H; R 5 and R 6 are each independently OH, OSO 2 CH 3 , O(CH 2 )mRe, CH 2 R f , OCOCH2OR g , OCH2CH2OR' or OCH2CH=CHR' , or together form OCH 2 0; Ra is H, or C 1 -6 20 alkyl; Rd is O or NCH 3 ; Re is H, halogen, C 3 - 6 cycloalkyl, naphthyl, N D N , , , or phenyl, which is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, OH, methoxy, CF 3 and COORa; R f is OCH2CH2R WO 2005/100303 PCT/KR2005/001066 74 -j-N /-\Rd or \- ; and R is phenyl.
3. The compound of claim 2, wherein R 1 is CH 3 ; R 2 is H, CN, CO 2 Ra or CONRbR; R 3 is C 1 - 6 alkyl, or phenyl, , , , , ,-N 5 or H , which is unsubstituted or substitutied with one or more halogens or C 1 - 6 alkyl groups; and R 5 and R 6 are each independently O(CH 2 )mRe or CH 2 R f , or together form OCH 2 0.
4. The compound of claim 1, which is selected from the group 10 consisting of: 1) 6-methoxy- 1l-(trans-methylimino-N-oxy)-3-phenyl- 1H-indene-2-carboxylate ethyl ester 2) 1-(trans-isopropylimino-N-oxy)-6-methoxy- 3 -phenyl- 1 H-indene-2 carboxylate ethyl ester 15 3) 1-(trans-benzylimino-N-oxy)-6-methoxy-3-phenyl-1H-indene-2-carboxylate ethyl ester 4) 1-(trans-ethylimino-N-oxy)-6-methoxy-3-phenyl- 1 H-indene-2-carboxylate ethyl ester 5) 6-methoxy-l-(trans-phenylpropylimino-N-oxy)-3-phenyl-1H-indene-2 20 carboxylate ethyl ester 6) 6-methoxy- 1l-(trans-(2-methylbutenylimino)-N-oxy)-3-phenyl- lH-indene-2 carboxylate ethyl ester 7) 1-(trans-isobutylimino-N-oxy)-6-methoxy-3-phenyl- 1 H-indene-2 carboxylate ethyl ester 25 8) 1-(trans-methy1imino-N-oxy)-6-(2-morphorline-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate ethyl ester WO 2005/100303 PCT/KR2005/001066 75 9) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 carboxylate ethyl ester 10) 1-(trans-methylimino-N-oxy)-6-phenetyloxy-3-phenyl- 1 H-indene-2 carboxylate ethyl ester 5 11) 3-furan-3-yl-l-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- lH indene-2-carboxylate ethyl ester 12) 6-hydroxy- 1-(trans-methylimino-N-oxy)-3-phenyl- 1H-indene-2 carboxylate ethyl ester 13) 1-(cis-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-1H-indene-2 10 carboxylate ethyl ester 14) 3-(trans-methylimino-N-oxy)- 1-phenyl-3H-indene-5-ol 15) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(5-phenylpentyloxy)- 1H-indene 2-carboxylate ethyl ester 16) 1-(cis-methylimino-N-oxy)-3-phenyl-6-(5-phenylpentyloxy)-1H-indene-2 15 carboxylate ethyl ester 17) 6-[2-(4-chlorophenoxy)acetoxy]-1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate ethyl ester 18) 6-[2-(4-chlorophenoxy)ethoxy]- 1l-(trans-methylimino-N-oxy)-3-phenyl- 1 H indene-2-carboxylate ethyl ester 20 19) 1-(trans-methylimino-N-oxy)-6-(naphthalene-2-ylmethoxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 20) methyl-[3-phenyl-6-(3-phenylpropoxy)indene-1-yllidene]amine-N-oxide 21) 1-(trans-methylimino-N-oxy)-6-[2-(5-methyl-2-phenylthiazol-4-yl)ethoxy] 3-phenyl-1H-indene-2-carboxylate ethyl ester 25 22) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-lH-indene-2 carboxylate ethyl ester 23) 6-[2-(4-hydroxyphenyl)ethoxy]-1 -(trans-methylimino-N-oxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 24) 6-(2-adaman- 1 -ylethoxy)- 1 -(trans-methylimino-N-oxy)-3-phenyl- 1 H 30 indene-2-carboxylate ethyl ester 25) 6-(2-cyclohexylethoxy)-1-(trans-methylimino-N-oxy)-3-phenyl- 1H-indene- WO 2005/100303 PCT/KR2005/001066 76 2-earboxylate ethyl ester 26) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(3-phenylprophenoxy)- 1H indene-2-carboxylate ethyl ester 27) 6-[2-(2-fluorophenyl)ethoxy]-l1-(trans-methylimino-N-oxy)-3-phenyl-l1H 5 indene-2-carboxylate ethyl ester 28) 6-[2-(3-fluorophenyl)ethoxy]-l1-(trans-methylimino-N-oxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 29) 6-[2-(4-fluorophenyl)ethoxy]-l1-(trans-methylimino-N-oxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 10 30) 1-(trans-methylimino-N-oxy)-3-phenyl-6-[2-(3 trifluoromethylphenyl)ethoxy]-1H-indene-2-carboxylate ethyl ester 31) 6-(4-methoxycarbonylbenzyloxy)-1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate ethyl ester 32) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 15 carboxylate ethyl amide 33) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate ethyl ester 34) 6-[2-(cyelohexylmethylamino)ethoxy]-l-(trans-methylimino-N-oxy)-3 phenyl-lH-indene-2-carboxylate ethyl ester 20 35) 3-(2-fluorophenyl)-6-methoxy- 1-(trans-methylimino-N-oxy)- 1H-indene-2 carboxylate ethyl ester 36) 1-(trans-methylimino-N-oxy)-6-[2-(4-methylpiperazine-1-yl)ethoxy]-3 phenyl- 1H-indene-2-carboxylate ethyl ester 37) (2,3-diphenyl indene-1-yl lidene)methylamine-N-oxide 25 38) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(3-phenylpropoxy)-l1H-indene-2 carboxylate isopropyl amide 39) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(3-phenylpropoxy)- 1 H-indene-2 carboxylate cyclohexyl amide 40) [1-(trans-methylimino-N-oxy)-3-phenyl- 6 -( 3 -phenylpropoxy)- lH-indene-2 30 yl]morpholine-4-yl-methanone 41) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-yl-ethoxy)-3-phenyl- 1 H- WO 2005/100303 PCT/KR2005/001066 77 indene-2-carboxylate cyclohexyl amide 42) 1-(trans-methylimino-N-oxy)-3-phenyl-5-(3-phenylpropoxy)- 1 H-indene-2 carboxylate ethyl ester 43) 1-(trans-methylimino-N-oxy)-6-phenethyloxymethyl- 3 -phenyl-lH-indene 5 2-carboxylate ethyl ester 44) (6-methoxy-3-phenylindene-1-yllidene)methylamine-N-oxide 45) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-1H indene-2-carboxylate ethyl ester 46) 6-(2-bromoethoxy)-l1-(trans-methylimino-N-oxy)- 3 -phenyl- 1H-indene-2 10 carboxylate ethyl ester 47) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-lH indene-2-carboxylate tert-buthyl ester 48) 1-(trans-methylimino-N-oxy)-5,6-methylenedioxy-1 -oxo-3-phenyl-lH indene-2-carboxylate ethyl ester 15 49) 4-[2-isopropylcarbamoyl-3-(trans-methylimino-N-oxy)-l1-phenyl-3H indene-5-yl-oxylmethyl]benzoate methyl ester 50) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-lH indene-2-carboxylate isopropyl amide 51) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-l1H 20 indene-2-carboxylate cyclopropyl amide 52) 3-(3-fluorophenyl)- 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 53) (6-methoxy- 1-(trans-methylimino-N-oxy)-3-phenyl- 1 H-indene-2-yl)acetate ethyl ester 25 54) (6-methoxy-l-(cis-methylimino-N-oxy)-3-phenyl-1H-indene-2-yl)acetate ethyl ester 55) 5-[2-(5-ethylpyridine-2-yl)ethoxy]- 1-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate isopropyl amide 56) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-p-tolyl- lH-indene-2 30 carboxylate ethyl ester 57) 1-(trans-methylimino-N-oxy)- 6 -( 3 -phenylpropoxy)-3-thiophene-2-yl-l1H- WO 2005/100303 PCT/KR2005/001066 78 indene-2-carboxylate ethyl ester 58) 3-(4-ehlorophenyl)- 1l-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1H indene-2-carboxylate ethyl ester 59) 3-(5-chlorothiophene-2-yl)-1-(trans-methylimino-N-oxy)-6-(3-phenyl 5 propoxy)-1H-indene-2-carboxylate ethyl ester 60) 1-(trans-methylimino-N-oxy)-6-( 3 -phenylpropoxy)-3-min-tolyl- 1H-indene-2 carboxylate ethyl ester 61) 1-(trans-methylimino-N-oxy)-3-(4-phenoxyphenyl)-6-(3-phenylpropoxy) 1H-indene-2-carboxylate ethyl ester 10 62) 3-benzo-[1,3]-dioxol-5-yl-l1-(trans-methylimino-N-oxy)-6-( 3 -phenyl propoxy)- 1H-indene-2-carboxylate ethyl ester 63) methyl-[6-(3-phenylpropoxy)-3-pyridine-2-yl-indene-1-yllidene]-amine-N oxide 64) 3-furan-2-yl- 1-(trans-methylimino-N-oxy)- 6 -( 3 -phenylpropoxy)- 1 H 15 indene-2-carboxylate ethyl ester 65) 3-ethyl- -(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)- 1H-indene-2 carboxylate ethyl ester 66) 3-methyl-l-(trans-methylimino-N-oxy)- 6 -( 3 -phenylpropoxy)-l1H-indene-2 carboxylate ethyl ester 20 67) 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-3-thiophene-3-yl-lH indene-2-carboxylate ethyl ester 68) 3-cyclopropyl-1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy)-1H indene-2-carboxylate ethyl ester 69) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-thiophene-3 25 yl-lH-indene-2-carboxylate ethyl ester 70) 3-benzo-[b]-thiophene-3-yl-l-(trans-methylimino-N-oxy)-6-(3-phenyl propoxy)-1H-indene-2-carboxylate ethyl ester 71) 3-(1H-imidazole-4-yl)- 1-(trans-methylimino-N-oxy)-6-(3-phenylpropoxy) 1H-indene-2-carboxylate ethyl ester 30 72) 3-(1-ethyl propyl)-1-(trans-methylimino-N-oxy)-6-( 3 -phenylpropoxy)-lH indene-2-carboxylate ethyl ester WO 2005/100303 PCT/KR2005/001066 79 73) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(3-phenylpropoxy)-l1H-indene-2 earboxylate amide 74) 6-(4-benzylmorpholine-2-ylmethoxy)-1-(trans-methylimino-N-oxy)- 3 phenyl-l1H-indene-2-carboxylate isopropyl amide 5 75) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(3-phenylpropoxy)- 1H-indene-2 carbonitrile 76) 1-(trans-methylimnino-N-oxy)-5,6-methylenedioxy-l1-oxo-3-phenyl-l1H phenyl-2-carboxylate isopropyl amide 77) 1-(trans-methylimino-N-oxy)-6-morpholine-4-ylmethyl-3-phenyl-lH 10 indene-2-carboxylate ethyl ester 78) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(2-pyridine-2-ylethoxy)-lH indene-2-carboxylate ethyl ester 79) 6-[2-(5-ethylpyridine-2-yl)ethoxy]-1-(trans-methylimino-N-oxy)- 3 -phenyl 1H-indene-2-carboxylate ethyl ester 15 80) 1-(trans-methylimino-N-oxy)- 3 -phenyl-6-(2-pyridine-2-ylethoxy)-l1H indene-2-carboxylate isopropyl amide 81) 6-[2-(5-ethylpyridine-2-yl)ethoxy]- l-(trans-methylimino-N-oxy)-3-phenyl 1H-indene-2-carboxylate isopropyl amide 82) methyl-[6-(2-morpholine-4-ylethoxy)- 3 -phenylindene-1-yllidene]amine-N 20 oxide 83) 5,6-bis-methanesulfonyloxy-l1-(trans-methylimino-N-oxy)- 3 -phenyl-1H indene-2-carboxylate ethyl ester 84) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-lH indene-2-carboxylate isobutyl ester 25 85) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate methyl ester 86) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-1H indene-2-carboxylate methyl ester 87) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl- 1H 30 indene-2-carboxylate propyl ester 88) 3-(4-fluorophenyl)- 1 -(trans-methylimino-N-oxy)-6-(2-morpholine-4- WO 2005/100303 PCT/KR2005/001066 80 ylethoxy)-1H-indene-2-carboxylate ethyl ester 89) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(pyridine-2-ylmethoxy)-l1H indene-2-carboxylate ethyl ester 90) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(pyridine-2-yloxy)- 1H-indene-2 5 carboxylate ethyl ester 91) 6-(3-methoxybenzyloxy)-l1-(trans-methylimino-N-oxy)-3-phenyl-lH indene-2-carboxylate ethyl ester 92) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)- 3 -thiophene-3 yl- 1H-indene-2-carboxylate isopropyl amide 10 93) 3-(1-ethylpropyl)-l-(trans-methylimino-N-oxy)-6-(2-morpholine- 4 -yl ethoxy)-1H-indene-2-carboxylate ethyl ester 94) 3-benzo-[b]-thiophene-3-yl- 1l-(trans-methylimino-N-oxy)-6-(2-morpholine 4-ylethoxy)-1H-indene-2-carboxylate isopropyl amide 95) 3-(4-fluorophenyl)- 1-(trans-methylimino-N-oxy)-6-(2-morpholine- 4 15 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 96) 3-(1-ethylpropyl)- 1-(trans-methylimino-N-oxy)-6-(2-morpholine- 4 ylethoxy)- 1H-indene-2-carboxylate isopropyl amide 97) 1-(trans-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-(2,4,6 trimethylphenyl)-IH-indene-2-carboxylate ethyl ester 20 98) 3-(2,6-dimethylphenyl)-1-(trans-methylimino-N-oxy)-6-(2-morpholine-4 ylethoxy)-1H-indene-2-carboxylate ethyl ester 99) 1-(trans-methylimino-N-oxy)-3-phenyl-5-(2-pyridine-2-ylethoxy)-l1H indene-2-carboxylate isopropyl amide 100) 1-(trans-methylimino-N-oxy)-5-(2-morpholine-4-ylethoxy)-3-phenyl- 1H 25 indene-2-carboxylate isopropyl amide 101) 1-(cis-methylimino-N-oxy)-6-(2-morpholine-4-ylethoxy)-3-phenyl-l1H indene-2-carboxylate isopropyl ester 102) 3-(3-fluorophenyl)- 1 -(trans-methylimino-N-oxy)-6-(2-pyridine-2 ylethoxy)-l1H-indene-2-carboxylate isopropyl amide 30 103) 6-[2-(5-ethylpyridine-2-yl)ethoxy]-3-(3-fluorophenyl)-l1-(trans methylimino-N-oxy)-1H-indene-2-carboxylate isopropyl amide WO 2005/100303 PCT/KR2005/001066 81 104) 3-(4-cyanophenyl)-6-(2-morpholine-4-ylethoxy)- 1-(trans-methylimino-N oxy)-1H-indene-2-carboxylate ethyl ester 105) 1-(trans-methylimino-N-oxy)-3-phenyl-6-(2-pyridine-2-ylethoxy)-1H indene-2-carboxylate isopropyl ester.
5. A process for preparing the indene derivative of claim 1, which comprises step of subjecting indenone compound of formula (II) to a condensation reaction with R 1 NHOH or NH20H to obtain a compound of formula (III), and reacting the compound of formula (TI) with R 1 X: 0 O' R 7 N"RI 6 RRs R7 0 R6 JR R 4 R (HI) HO R 7 N I . / R 2 R4 R$ 15 wherein, X is halogen; R 1 is C1- 6 alkyl, C1-. 6 alkenyl or C 3 -6 cycloalkyl, which is unsubstituted or substitutied with one or more phenyl groups; WO 2005/100303 PCT/KR2005/001066 82 0 R 2 is H, CN, CO 2 Ra, CH 2 CO 2 Ra, CONRbRc, Rd ,or phenyl; R 3 is C1- 6 alkyl, C 3 -6 cycloalkyl, or naphthyl, phenyl, 0 S S Sor H , which is unsubstituted or substitutied with one or more substituents selected from the group consisting of halogen, CN, 5 NH 2 , NO 2 , ORa, phenyloxy, C1- 6 alkyl and C 3 .- 6 cycloalkyl; and R 4 , Rs, R 6 and R 7 are each independently H, OH, OSO 2 CH 3 , O(CH 2 ) 1 Re, CH 2 R', OCOCH 2 OR g , OCH2CH2OR' or OCH2CH=CHR , or Rs and R 6 together form OCH 2 0; in which Ra is H, or C 1 - 6 alkyl or C 3 - 6 cycloalkyl, which is unsubstituted 10 or substitutied with one or more halogens; Rb and Re are each independently H, C 1 .- 6 alkyl or C 3 - 6 cycloalkyl; Rd is O, S or NRa; Re is H, halogen, C 3 - 6 cycloalkyl, naphthyl, R a Rd N ,or phenyl, which is 15 unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, CN, NH 2 , NO 2 , OR a , CF 3 and COORa; j-N R\ R f is OCHzCH 2 R g or R9 is phenyl, which is unsubstituted or substituted with one or more substituents selected from the group consisting of halogen, CN, NH 2 , NO 2 and 20 ORa; and m is an integer in the range of 1 to 5. WO 2005/100303 PCT/KR2005/001066 83
6. The process of claim 5, wherein the indenone compound of formula (II) is prepared by a process comprising the steps of: 1) reacting compounds of formula (V) and (VI) to obtain a compound of formula (VII); 5 2) subjecting the compound of formula (VII) to cyclization to obtain a compound of formula (VIII); and 3) subjecting the compound of formula (VIII) to oxidation. O Re(V) R7 R6 z R4 10 (VI) 7 Re R 2 R5" # o" R3 R4(VII) R O R 2 Rtj) (VII) wherein, R 2 to R 7 have the same meanings as defined in claim 5, and Z is halogen 15 or activated leaving group.
7. The process of claim 5, wherein the indenone compound of formula (II) is prepared by a process comprising the steps of: WO 2005/100303 PCT/KR2005/001066 84 1) reacting compounds of formula (IX) and (X) to obtain a compound of formula (XI); 2) subjecting the compound of formula (XI) to cyclization to obtain a compound of formula (XII); and 5 3) subjecting the compound of formula (XII) to oxidation. R4 7 0 (IX) o R5 I' (X) R 7 0 Re R 2 R4 (XI) I _R2 R 7 0 R 6 R3 R 4 (XII) 10 wherein, R 2 to R 7 have the same meanings as defined in claim 5.
8. The process of claim 5, wherein the indenone compound of formula (II) is prepared by a process comprising the steps of: 15 1) reacting compounds of formula (IX) and (XIII) to obtain a compound of formula (XIV); and 2) subjecting the compound of formula (XIV) to cyclization. WO 2005/100303 PCT/KR2005/001066 85 Re R 2 I R 4 (IX) O R3 CI (XIII) R 7 R5 0 R3 R 4 (XIV) wherein, 5 R 2 to R 7 have the same meanings as defined in claim 5.
9. The process of claim 5, wherein the indenone compound of formula (II) is prepared by a process comprising the steps of: 1) subjecting a compound of formula (XV) to bromination obtain a 10 compound of formula (XVI); and 2) subjecting the compound of formula (XVI) to a carbon-carbon coupling reaction in the presence of a metal catalyst, or to a substitution reaction using a nucleophile. R 7 0 Re R 4 R3 (XV) R 7 0 Ra Br R 5 R 4 Ra 15 (XVI) wherein, WO 2005/100303 PCT/KR2005/001066 86 R 3 to R 7 have the same meanings as defined in claim 5.
10. The process of claim 5, wherein the indenone compound of formula (II) is prepared by a process comprising the steps of: 5 1) subjecting a compound of formula (XVII) to bromination obtain a compound of formula (XVIII); and 2) subjecting the compound of formula (XVIII) to a carbon-carbon coupling reaction in the presence of a metal catalyst, or to a substitution reaction using a nucleophile. R 7 0 RR2 10 R4 (XVII) R 7 0 R 6 /R 2 Br (XVIII) wherein, R 2 and R 4 to R 7 have the same meanings as defined in claim 5. 15
11. The process of claim 5, wherein the indenone compound of formula (II) is prepared by subjecting a compound of formula (XIX) to an acylation reaction, a halogenation reaction followed by a substitution reaction by a nucleophile, or a carbon-carbon coupling reaction in the presence of a metal catalyst. 0 -(CH 2 )n- R 2 R3 20 (XIX) wherein, WO 2005/100303 PCT/KR2005/001066 87 R 2 and R 3 have the same meanings as defined in claim 5, Y is hydroxy, thiol, amino C 1 I-6 alkyl or halogen, and n is an integer in the range of 0 to 5.
12. A pharmaceutical composition for modulating the activities of 5 peroxisome proliferator activated receptors (PPARs) comprising a therapeutically effective amount of the compound or salt defined in claim 1 as an active ingredient together with a pharmaceutically acceptable carrier.
13. The composition of claim 12, which is used for the treatment and 10 prevention of diabetes, obesity, arteriosclerosis, hyperlipidemia, hyperinsulinism, hypertension, osteoporosis, liver cirrhosis, asthma and cancer.
AU2005233039A 2004-04-13 2005-04-13 Indene derivatives and process for the preparation thereof Ceased AU2005233039B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
KR1020040025217A KR100592805B1 (en) 2004-04-13 2004-04-13 Indene derivatives and process for the preparation thereof
KR10-2004-0025217 2004-04-13
PCT/KR2005/001066 WO2005100303A1 (en) 2004-04-13 2005-04-13 Indene derivatives and process for the preparation thereof

Publications (2)

Publication Number Publication Date
AU2005233039A1 true AU2005233039A1 (en) 2005-10-27
AU2005233039B2 AU2005233039B2 (en) 2008-03-13

Family

ID=35149926

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2005233039A Ceased AU2005233039B2 (en) 2004-04-13 2005-04-13 Indene derivatives and process for the preparation thereof

Country Status (11)

Country Link
US (1) US7741323B2 (en)
EP (1) EP1740531A4 (en)
JP (1) JP4459268B2 (en)
KR (1) KR100592805B1 (en)
CN (1) CN1942434B (en)
AU (1) AU2005233039B2 (en)
BR (1) BRPI0509794A (en)
CA (1) CA2563000C (en)
HK (1) HK1102395A1 (en)
MX (1) MXPA06011513A (en)
WO (1) WO2005100303A1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2913019A1 (en) * 2007-02-23 2008-08-29 Cerep Sa New substituted heterocyclic compounds useful for treating/preventing cancer e.g. prostate, lung, breast, colon, skin, kidney and bone cancer, psoriasis, rheumatoid arthritis, Kaposis sarcoma, atherosclerosis and autoimmune diseases
KR101149529B1 (en) * 2009-09-11 2012-05-25 한국화학연구원 Indenone derivatives and pharmaceutical composition comprising the same
KR101295375B1 (en) * 2011-03-30 2013-08-13 한국화학연구원 Novel inden derivatives substituted with alkyl group containing pyridine, pharmaceutically acceptable salts or isomer thereof, process for the preparation thereof and pharmaceutical composition for prevention or treatment of PAR-1 related diseases containing the same as an active ingredient
KR101423228B1 (en) 2012-08-22 2014-07-24 한국화학연구원 A composition for promoting differentiation comprising indenone derivatives or pharmaceutically acceptable salt thereof
US11053189B2 (en) 2019-03-25 2021-07-06 National Tsing Hua University Method and mixture to form functionalized cyclic compounds
KR102412252B1 (en) * 2019-11-07 2022-06-23 서울대학교산학협력단 Pharmaceutical composition for preventing or treating thrombotic disease comprising indene n-oxide derivative
CN113105368A (en) * 2021-04-16 2021-07-13 安徽大学 Synthesis method of N-aryl nitrone derivative
WO2024005578A1 (en) * 2022-06-29 2024-01-04 아밀로이드솔루션 주식회사 Novel indenone derivatives and uses thereof

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH06239812A (en) * 1993-02-16 1994-08-30 Otsuka Pharmaceut Co Ltd Production of 1-amino-2,3-dihydro-7-hydroxy-1h-indene derivative
JPH06298711A (en) * 1993-04-13 1994-10-25 Otsuka Pharmaceut Co Ltd Production of optically active 2,3-dihydro-1h-indene derivative
EP0874059A4 (en) 1996-01-12 1999-10-27 Nippon Steel Chemical Co Processes for producing indane derivatives
EP1132389A1 (en) * 2000-03-06 2001-09-12 Vernalis Research Limited New aza-indolyl derivatives for the treatment of obesity
CN1430603A (en) * 2000-04-28 2003-07-16 旭化成株式会社 Novel bicyclic compounds
CA2427499A1 (en) * 2000-10-10 2002-04-18 Smithkline Beecham Corporation Substituted indoles, pharmaceutical compositions containing such indoles and their use as ppar-.gamma. binding agents
KR100595963B1 (en) * 2004-04-13 2006-07-05 한국화학연구원 Indene derivatives and process for the preparation thereof

Also Published As

Publication number Publication date
US7741323B2 (en) 2010-06-22
HK1102395A1 (en) 2007-11-16
MXPA06011513A (en) 2007-07-04
KR20050100051A (en) 2005-10-18
CN1942434B (en) 2011-07-06
EP1740531A1 (en) 2007-01-10
CA2563000A1 (en) 2005-10-27
WO2005100303A1 (en) 2005-10-27
KR100592805B1 (en) 2006-06-26
JP2007532635A (en) 2007-11-15
EP1740531A4 (en) 2012-02-29
BRPI0509794A (en) 2007-10-23
CA2563000C (en) 2011-06-21
JP4459268B2 (en) 2010-04-28
US20070185109A1 (en) 2007-08-09
AU2005233039B2 (en) 2008-03-13
CN1942434A (en) 2007-04-04

Similar Documents

Publication Publication Date Title
CA2563000C (en) Indene derivatives and process for the preparation thereof
JP5254228B2 (en) Novel compounds, isomers or pharmaceutically acceptable salts thereof as vanilloid receptor antagonists; and pharmaceutical compositions containing the same
WO2004007439A1 (en) Biaryl derivatives
AU2009263384A1 (en) Carboxylic acid compound
JP5208239B2 (en) Novel production method of anticancer active tricyclic compounds by alkyne coupling
JP2839805B2 (en) Lignan analog, method for producing the same, and antihyperlipidemic agent
JP2007197324A (en) 2,4,5-substituted-1,3-azole derivative
JPH06306038A (en) Cyclopropyl derivative lipoxygenase inhibitor
CA1319689C (en) Substituted alkylamine derivatives
US5116855A (en) Rhodanine derivatives and pharmaceutical compositions
US4146385A (en) Derivatives of phenoxyalkylcarboxylic acids
US7745439B2 (en) Indene derivatives and process for the preparation thereof
AU2005302409A1 (en) Substituted carboxylic acids
JP4094955B2 (en) Terphenyl compound having a substituted amino group
US20030083357A1 (en) Oxime derivatives for the treatment of dyslipidemia and hypercholesteremia
DK159435B (en) METHOD OF ANALOGUE FOR PREPARING 2-HYDROXY-5- (1-HYDROXY-2-PIPERAZINYLETHYL) BENZOIC ACID DERIVATIVES OR A PHARMACEUTICAL ACCEPTABLE ACID ADDITION SALT
EA009700B1 (en) Non-nucleotide reverse transcriptase inhibitors
SU692561A3 (en) Method of preparing 2-nitro-8-phenylbenzofuran derivatives
US20040162331A1 (en) Pyrrole derivative
EP2114875B1 (en) Substituted arylcylopentenes as therapeutic agents
JP3245862B2 (en) Novel sulfonic acid derivatives and their pharmaceutical uses
CA2098366A1 (en) Substituted (benzothiazolyl- and quinoxalyl-methoxy) phenyl-acetic acid derivatives
KR101916106B1 (en) Synthetic method for 2,5-diaryloxazole compounds and anti-inflammatory pharmaceutical compounds containing the 2,5-diaryloxazole compounds
JP3149279B2 (en) Cyclopropenone derivative
US5190971A (en) Substituted dibenz-oxa-thiocinones, -12-oxides and -12,12-dioxides, a process for their preparation and their use in medicaments

Legal Events

Date Code Title Description
FGA Letters patent sealed or granted (standard patent)
MK14 Patent ceased section 143(a) (annual fees not paid) or expired